Monday, 26 March 2012

Ala-Seb-T Shampoo


Pronunciation: kole tar/SAL-i-SIL-ik AS-id/SUL-fur
Generic Name: Coal Tar/Salicylic Acid/Sulfur
Brand Name: Examples include Ala-Seb-T and Pazol XS


Ala-Seb-T Shampoo is used for:

Relieving itching, flaking, irritation, redness, and scaling caused by dandruff, seborrheic dermatitis, and psoriasis of the scalp. It may also be used for other conditions as determined by your doctor.


Ala-Seb-T Shampoo is a topical coal tar, salicylate, and sulfur combination. It works by causing the skin to swell, soften, and then slough or peel in areas where it is applied.


Do NOT use Ala-Seb-T Shampoo if:


  • you are allergic to any ingredient in Ala-Seb-T Shampoo

  • you are using prescription medicine or other treatments for psoriasis (eg, ultraviolet radiation therapy), unless instructed by your doctor

Contact your doctor or health care provider right away if any of these apply to you.



Before using Ala-Seb-T Shampoo:


Some medical conditions may interact with Ala-Seb-T Shampoo. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

  • if you have liver or kidney problems, a skin infection, skin irritation, eczema, diabetes, or poor blood circulation

Some MEDICINES MAY INTERACT with Ala-Seb-T Shampoo. Because little, if any, of Ala-Seb-T Shampoo is absorbed into the blood, the risk of it interacting with another medicine is low.


Ask your health care provider if Ala-Seb-T Shampoo may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Ala-Seb-T Shampoo:


Use Ala-Seb-T Shampoo as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Shake well before each use.

  • Wet hair, apply generously, and massage onto wet scalp. Leave lather on your scalp for a full 5 minutes. Rinse well and repeat. Be sure to wash your hands after each use.

  • If you miss a dose of Ala-Seb-T Shampoo, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Ala-Seb-T Shampoo.



Important safety information:


  • Ala-Seb-T Shampoo is for external use only. Avoid getting Ala-Seb-T Shampoo in your eyes, nose, or mouth, or on the genitals. If contact with your eyes occurs, flush with water for 15 minutes. Do not inhale the vapors of Ala-Seb-T Shampoo.

  • Ala-Seb-T Shampoo may cause harm if it is swallowed. If you may have taken it by mouth, contact your poison control center or emergency room right away.

  • Overuse of topical products may worsen your condition. Do NOT use more than the recommended dose of Ala-Seb-T Shampoo. Do not use for longer than prescribed by your doctor or on the package label without checking with your doctor.

  • If your condition does not get better after regular use of Ala-Seb-T Shampoo or if it gets worse, check with your doctor.

  • Check with your doctor before use if you have a condition that covers a large area of the body.

  • Be sure to apply Ala-Seb-T Shampoo only to the affected area and not to normal healthy skin.

  • Do not use Ala-Seb-T Shampoo on skin that is irritated, infected, or reddened.

  • Do not use Ala-Seb-T Shampoo on open skin wounds, moles, birthmarks, genital warts, warts on the face, or warts growing hair.

  • Do not use any other medicines or drying products on your skin unless your doctor instructs you otherwise.

  • Ala-Seb-T Shampoo may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Ala-Seb-T Shampoo. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • Ala-Seb-T Shampoo contains a salicylate, which has been linked to Reye syndrome. Do not use Ala-Seb-T Shampoo on children or teenagers during or after chickenpox, flu, or other viral infections without checking with your doctor or pharmacist.

  • Ala-Seb-T Shampoo should not be used in CHILDREN younger than 2 years old unless your doctor tells you otherwise.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Ala-Seb-T Shampoo during pregnancy. It is not known if Ala-Seb-T Shampoo is found in breast milk. Do not breast-feed while you are using Ala-Seb-T Shampoo.


Possible side effects of Ala-Seb-T Shampoo:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Dry, peeling, red, or scaling skin.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); severe irritation.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Ala-Seb-T side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include agitation; diarrhea; dizziness; loss of appetite; loss of hearing; mental disturbances; nausea; rapid or difficult breathing; ringing in the ears; seizures; sluggishness; vomiting; yellowing of the skin or eyes.


Proper storage of Ala-Seb-T Shampoo:

Store Ala-Seb-T Shampoo at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not freeze. Do not store in the bathroom. Keep Ala-Seb-T Shampoo out of the reach of children and away from pets.


General information:


  • If you have any questions about Ala-Seb-T Shampoo, please talk with your doctor, pharmacist, or other health care provider.

  • Ala-Seb-T Shampoo is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Ala-Seb-T Shampoo. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Ala-Seb-T resources


  • Ala-Seb-T Side Effects (in more detail)
  • Ala-Seb-T Use in Pregnancy & Breastfeeding
  • Ala-Seb-T Drug Interactions
  • 0 Reviews · Be the first to review/rate this drug

mesna


Generic Name: mesna (MEZ nah)

Brand Names: Mesnex


What is mesna?

Mesna is detoxifying agent. It reduces the harmful effects of certain metabolites (breakdown products) of the cancer chemotherapy medicine ifosfamide (Ifex).


Mesna is used to prevent bleeding in the bladder (hemorrhagic cystitis) during chemotherapy with ifosfamide (Ifex).


Mesna may also be used for purposes other than those listed here.


What is the most important information I should know about mesna?


It is important to drink at least one quart (4 cups) of liquid each day during treatment with mesna, whether it is taken by mouth or by injection.


If you see blood in the urine or notice that it has a pink or red color, contact your doctor as soon as possible. Some foods or dyes may cause a red color in the urine, however it will be necessary to determine if the color is due to blood in the urine.

What should I discuss with my healthcare provider before taking mesna?


Do not take mesna without first talking to your doctor if you have

  • had a previous allergic reaction to mesna or to another medicine that contains sulfur; or




  • an autoimmune disorder such as rheumatoid arthritis, systemic lupus erythematosus (SLE), or nephritis (a type of kidney problem).



You may not be able to take mesna, or you may require a dosage adjustment or special monitoring during treatment.


Mesna is in the FDA pregnancy category B. This means that it is not expected to be harmful to an unborn baby. Do not take mesna without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether mesna passes into breast milk. Do not take mesna without first talking to your doctor if you are breast-feeding a baby.

How should I take mesna?


Take mesna exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Take each oral dose with a full glass of water.

If vomiting occurs within 2 hours of taking a dose of mesna, contact your healthcare provider.


Mesna is also available as an injection. Your healthcare provider will administer injectable mesna. If you are using injectable mesna at home, your healthcare provider will give you detailed instructions regarding preparation, administration, and storage of the medication.


It is important to drink at least one quart (4 cups) of liquid each day during treatment with mesna, whether it is taken by mouth or by injection.


A small number of patients who take mesna get blood in the urine (hematuria). Your doctor will check your urine each day that mesna is taken. Laboratory tests can detect blood in the urine that is not visible just by looking at it.


If you see blood in the urine or notice that it has a pink or red color, contact your doctor as soon as possible. Some foods or dyes may cause a red color in the urine, however it will be necessary to determine if the color is due to blood in the urine. Store mesna at room temperature away from moisture and heat.

See also: Mesna dosage (in more detail)

What happens if I miss a dose?


Contact your healthcare provider if a dose of mesna is missed.


What happens if I overdose?


Seek emergency medical attention if an overdose is suspected.

Symptoms of a mesna overdose may include diarrhea, tremor, seizures, shortness of breath, and bluish color of the skin.


What should I avoid while taking mesna?


There are no restrictions on foods, beverages, or activities during treatment with mesna unless otherwise directed by your doctor.


Mesna side effects


Seek emergency medical attention or contact your healthcare provider immediately if you experience any of the following serious side effects:

  • an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives); or




  • pink or red colored urine.



Other less serious side effects may be more likely to occur. Continue to take mesna, and contact your doctor if you experience any of the following side effects:



  • nausea or vomiting;




  • decreased appetite;




  • stomach pain;




  • diarrhea;




  • dizziness;




  • flushing;




  • fever;




  • sensitive skin or skin rash;




  • paleness of the skin;




  • sleepiness;




  • coughing or cold symptoms;




  • pain, redness, or irritation at the injection site;




  • swelling or water retention; or




  • low blood pressure.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.


Mesna Dosing Information


Usual Adult Dose for Hemorrhagic Cystitis Prophylaxis:

Prevention of ifosfamide-induced cystitis:
Mesna may be given on a fractionated dosing schedule of either 3 bolus intravenous injections or a single injection followed by two oral doses. IV mesna is administered at 20% of the ifosfamide dose while oral mesna is administered at 40% of the ifosfamide dose.

IV: 20% of the ifosfamide dose once at the time of ifosfamide administration and 20% of the ifosfamide dose 4 and 8 hours after each dose of ifosfamide. Thus, if ifosfamide were given at 1.2 g/m2, the dose of mesna would be 240 mg/m2 given at 0, 4, and 8 hours after ifosfamide.

When given with a continuous infusion of ifosfamide, mesna may be dosed on a "mg per mg" basis (e.g., 1.2 g/m2 for a 1.2 g/m2 continuous infusion of ifosfamide). 10% of the dose should be given before the ifosfamide infusion and the remainder continued during and for 12 to 24 hours after the ifosfamide infusion has stopped.

Oral (to be given after one dose of IV mesna): 40% of the ifosfamide dose at 2 and 6 hours after each dose of ifosfamide. Thus, if ifosfamide were given at 1.2 g/m2, the dose of IV mesna would be 240 mg/m2 given at the time of ifosfamide administration and the dose of oral mesna would be 480 mg/m2 given at 2 and 6 hours after ifosfamide.

Usual Pediatric Dose for Hemorrhagic Cystitis Prophylaxis:

Prevention of ifosfamide-induced cystitis:
Mesna may be given on a fractionated dosing schedule of either 3 bolus intravenous injections or a single injection followed by two oral doses. IV mesna is administered at 20% of the ifosfamide dose while oral mesna is administered at 40% of the ifosfamide dose.

IV: 20% of the ifosfamide dose once at the time of ifosfamide administration and 20% of the ifosfamide dose 4 and 8 hours after each dose of ifosfamide. Thus, if ifosfamide were given at 1.2 g/m2, the dose of mesna would be 240 mg/m2 given at 0, 4, and 8 hours after ifosfamide.

When given with a continuous infusion of ifosfamide, mesna may be dosed on a "mg per mg" basis (e.g., 1.2 g/m2 for a 1.2 g/m2 continuous infusion of ifosfamide). 10% of the dose should be given before the ifosfamide infusion and the remainder continued during and for 12 to 24 hours after the ifosfamide infusion has stopped.

Oral (to be given after one dose of IV mesna): 40% of the ifosfamide dose at 2 and 6 hours after each dose of ifosfamide. Thus, if ifosfamide were given at 1.2 g/m2, the dose of IV mesna would be 240 mg/m2 given at the time of ifosfamide administration and the dose of oral mesna would be 480 mg/m2 given at 2 and 6 hours after ifosfamide.


What other drugs will affect mesna?


It is not known whether other medicines will interact with mesna. Talk to your doctor and pharmacist before taking any other prescription or over-the-counter medicines, including vitamins, minerals and herbal products.



More mesna resources


  • Mesna Side Effects (in more detail)
  • Mesna Dosage
  • Mesna Use in Pregnancy & Breastfeeding
  • Mesna Drug Interactions
  • Mesna Support Group
  • 0 Reviews for Mesna - Add your own review/rating


  • mesna Intravenous Advanced Consumer (Micromedex) - Includes Dosage Information

  • Mesna Prescribing Information (FDA)

  • Mesna Professional Patient Advice (Wolters Kluwer)

  • Mesna Monograph (AHFS DI)

  • Mesna MedFacts Consumer Leaflet (Wolters Kluwer)

  • Mesnex Prescribing Information (FDA)

  • Mesnex MedFacts Consumer Leaflet (Wolters Kluwer)



Compare mesna with other medications


  • Hemorrhagic Cystitis Prophylaxis


Where can I get more information?


  • Your pharmacist has more information about mesna written for health professionals that you may read.

See also: mesna side effects (in more detail)


Wednesday, 21 March 2012

Aluminum Chloride Hexahydrate topical


Class: Astringents
VA Class: DE450
Chemical Name: Aluminum chloride, hexahydrate
Molecular Formula: AlCl3•6H2O
CAS Number: 7784-13-6, 7446-70-0
Brands: Certain Dri, Drysol, Hypercare, Xerac AC

Introduction

Antiperspirant.2 11 13 14 15


Uses for Aluminum Chloride Hexahydrate


Hyperhidrosis


Topical treatment of hyperhidrosis.1 2 4 5 6 7 8 9 10 11 13 14 15


Hyperhidrosis (excessive sweating) may be primary (physiologic, idiopathic, essential; possibly hereditary) or secondary (associated with an underlying condition).5 7 8 9 10 14 Secondary hyperhidrosis is associated with neurologic, endocrinologic, metabolic, or other such disorders; febrile illness; malignancy; or drugs.5 7 8 9 10 14


Hyperhidrosis is classified as focal or generalized.5 Focal hyperhidrosis most commonly affects the palms and soles (palmar-plantar hyperhidrosis) and underarms (axillary hyperhidrosis), and least commonly affects the face (craniofacial hyperhidrosis).5 7 8 9 10 14 Generalized hyperhidrosis involves the entire body and usually is associated with an underlying condition.10


Generally considered first-line therapy for mild or moderate primary focal hyperhidrosis, including axillary5 7 8 10 11 13 14 and palmar-plantar hyperhidrosis.7 8 10 11 14 An adequate trial of topical aluminum chloride usually is recommended before other therapeutic options (e.g., botulinum toxin injections, iontophoresis, local excision, liposuction, sympathectomy) considered.7 8 9 10 11 In severe cases of axillary, palmar, or plantar hyperhidrosis, some clinicians state that aluminum chloride hexahydrate, botulinum toxin injections, or iontophoresis are considered first-line therapy.8


One of several options for treatment of craniofacial hyperhidrosis.1 7 8


Self-medication (Certain Dri, OTC use) for axillary hyperhidrosis only.15


Aluminum Chloride Hexahydrate Dosage and Administration


Administration


Topical Administration


Preparations are for external use only.1 2 4 15


Apply topically to the skin as a solution1 2 4 or as an antiperspirant stick.15


Avoid contact with eyes.1 2 4 7 15 If contact occurs, wash affected eye(s) thoroughly with water.1 2


Apply to dry, intact skin only; do not apply to any irritated, broken, or recently shaven areas.1 2 4 5 6 7 8 9 11 15 May use a hairdryer on warm setting to dry the skin.1 2


Do not apply other deodorants or antiperspirants to treatment area.1 2


For optimum effect, apply at bedtime when sweat glands are least active.1 2 4 8 9 10 11 13 15


Apply solution using fingers, moistened cotton ball, or applicator (Dab-O-Matic) supplied by manufacturer.1 2 4 If using the Dab-O-Matic applicator, remove and discard protective cap prior to use.1 2 4 Push applicator into bottle and twist white cap to secure in place.2 4


Consult individual manufacturer’s prescribing or patient information for complete instructions regarding proper drug application and removal.1 2 4 7 15


Dosage


Adults


Hyperhidrosis

Axillary, Palmar, Plantar, or Craniofacial Hyperhidrosis

Topical

Apply solution to completely dry affected area (e.g., underarms, palms, soles, scalp) once daily at bedtime.1 2 4 5 7 8 9 11


To minimize irritation when using the solution, let alcohol evaporate1 2 (may use a hairdryer on cold setting when administered under arms);1 a thin film of drug should remain on skin.1 2


To prevent drug from rubbing off, cover treated area with a T-shirt for axillary application;1 2 4 5 use a plastic shower cap for scalp application1 5 or plastic wrap and overlying gloves or socks for palmar or plantar application, respectively.1 4 5 14 Do not use adhesive tape.1 4 Some clinicians state that occlusion is not necessary and may increase risk of skin irritation.9 11 (See Dermatologic Effects under Cautions.)


After 6–8 hours (usually the following morning), remove garments and/or plastic wrap; to prevent irritation, wash treatment area(s) thoroughly with soap and water or shampoo.1 2 4 5 6 7 9 10 14 Some clinicians also suggest topical application of sodium bicarbonate.6 Dry with towel.1


Repeat applications for ≥2 consecutive nights until desired effect (lack of sweating) achieved.1 4 5 6 7 9 11 Thereafter, may apply additional treatments once or twice weekly as needed.1 4 5 9


Self-medication for Axillary Hyperhidrosis

Topical

Apply sparingly (i.e., a few strokes) to affected areas under each arm.15 Dry skin completely prior to application.15


Allow solution to dry following application.15


May repeat treatment until desired effect achieved.15 Thereafter, apply every other day or as needed.15


Cautions for Aluminum Chloride Hexahydrate


Contraindications



  • Known hypersensitivity to aluminum chloride hexahydrate or any ingredient in the formulation.6



Warnings/Precautions


Warnings


Administration

Self-medication: Apply Certain Dri to underarms only.15 (For further information on warnings and precautions associated with administration of aluminum chloride hexahydrate (Drysol, Xerac AC, and Hypercare) and aluminum chloride [Certain Dri], see Topical Administration under Dosage and Administration.)


Flammability

Aluminum chloride solutions are flammable; do not use near an open flame.1 2 4


Sensitivity Reactions


Dermatologic Effects

Possible local irritation (e.g., burning, stinging, itching, tingling);1 2 4 7 8 10 13 14 usually resolves with temporary discontinuance of drug.1 2 4 Because risk of skin sensitivity increases with higher concentrations, some patients may benefit from an initial trial with reduced concentrations (10–12%) of aluminum chloride hexahydrate.7 8


To minimize skin irritation, follow specific instructions provided by each manufacturer on proper drug application and removal.1 2 4 7 10 Ensure that skin is completely dry prior to and following drug application.1 2 4 5 7 9 11 15 (See Topical Administration under Dosage and Administration.)


If rash or skin reaction develops during therapy, discontinue use and consult a clinician.1 2 4 15 Topical sodium bicarbonate or a low-dose corticosteroid cream (e.g., 1% hydrocortisone) may be used to limit or treat irritation.6 7 9 11 14 Other measures include decreasing concentration or frequency of applications.7 If persistent skin irritation occurs, refer patient to a dermatologist.7


General Precautions


Fabric or Metal Stains

May be harmful to certain fabrics (e.g., cotton) or metals.1 2 4 11 13 15 Allow skin to dry completely following application and thoroughly wash off any residual drug after 6–8 hours of treatment to avoid damage to clothing.1 15


Specific Populations


Pregnancy

The manufacturer of Drysol and Xerac AC states that there is no pregnancy category for these drugs; however, they recommend that the drug not be used in pregnant women.3


Pediatric Use

Keep preparations out of reach of children.1 2 4 15 16


Infants (especially preterm infants) and children may be at greater risk of aluminum exposure because of immature renal function.16


Renal Impairment

Possible increased exposure to any systemically absorbed aluminum in patients with renal impairment; patients with renal impairment should consult a clinician before use.16 (See Bioavailability and Special Populations under Pharmacokinetics.)


Common Adverse Effects


Local skin irritation (burning, stinging, itching, tingling).1 7 8 10 11 13 14


Aluminum Chloride Hexahydrate Pharmacokinetics


Absorption


Bioavailability


One manufacturer states that drug is not absorbed; however, some clinicians state that minimal systemic absorption may occur when applied topically.16 17


Onset


Following topical application of aluminum chloride hexahydrate 20% solution to the palms, reduced sweating occurs within 48 hours.10 14


Duration


Following topical application of aluminum chloride hexahydrate 20% to the palms, effects of reduced sweating diminish or disappear within 48 hours after discontinuance of therapy.10 14


Elimination


Elimination Route


Absorbed aluminum is eliminated principally by the kidneys.17


Special Populations


Renal impairment: Possible decreased clearance and increased exposure to any absorbed aluminum.16 17


Stability


Storage


Topical


Solution

15–30°C,4 in tightly closed container when not in use (to prevent evaporation).1 2 4


Keep away from open flames.1 2 4


ActionsActions



  • Pathophysiology of focal hyperhidrosis is poorly understood.8 10




  • Eccrine (sweat) glands are distributed over nearly the entire body surface with high concentrations in palms, soles, and forehead.8 These glands are innervated by cholinergic fibers of the sympathetic nervous system.8 9 10




  • Since patients with focal hyperhidrosis do not have any histopathologic changes in sweat glands or in their numbers, it has been suggested that a complex dysfunction of the sympathetic nervous system is likely to contribute to hyperhidrosis.8 10




  • Mechanically blocks eccrine sweat gland ducts,5 6 7 9 10 12 13 14 possibly by forming aluminum ion precipitate complexes within the acrosyringium (most superficial) portion of eccrine glands.12




  • Long-term (≥6 months) use appears to cause dilation and atrophy of secretory cells within eccrine sweat glands.5 12 13 14




  • Does not appear to affect apocrine glands.12



Advice to Patients



  • Importance of avoiding contact with eyes.1 2 4 15 If ocular contact occurs, rinse eye(s) thoroughly with water.1 2




  • Importance of instructing patients on proper technique for application and removal of drug.1 2 4 7 15




  • Importance of discontinuing therapy and informing clinician if a rash or skin reaction occurs.1 2 4 15




  • Importance of patients with renal impairment consulting a clinician before starting or continuing to use antiperspirants containing aluminum because of possible increased exposure to any absorbed aluminum.16




  • Importance of informing clinician if accidental ingestion occurs in a pediatric patient.16




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1 2 4 15




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.1 2 4 15




  • Importance of informing patients of other important precautionary information.1 2 4 15 (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.













Aluminum Chloride

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Topical



Stick



12%



Certain Dri



DSE Healthcare Solutions























Aluminum Chloride Hexahydrate

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Topical



Solution



6.25%



Xerac AC (with anhydrous ethyl alcohol 96%)



Person and Covey



20%



Drysol (with anhydrous ethyl alcohol 93%)



Person and Covey



Hypercare



Stratus



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions March 2009. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



1. Person and Covey, Inc. Drysol (aluminum chloride hexahydrate) solution prescribing information. Glendale, CA; 2001 Sep 27.



2. Person and Covey, Inc. Xerac AC (aluminum chloride hexahydrate) solution prescribing information. Glendale, CA; 2001 Sep 24.



3. Person and Covey, Glendale,CA: Personal communication.



4. Stratus Pharmaceuticals, Inc. Hypercare (aluminum chloride hexahydrate) solution prescribing information. Miami, FL; undated.



5. Eisenach JH, Atkinson JLD, Fealey RD. Hyperhidrosis: evolving therapies for a well-established phenomenon. Mayo Clin Proc. 2005; 80:657-66. [PubMed 15887434]



6. Thomas I, Brown J, Vafaie J et al. Palmoplantar hyperhidrosis: a therapeutic challenge. Am Fam Physician. 2004; 69:1117-20. [PubMed 15023010]



7. Hornberger J, Grimes K, Naumann M et al. Recognition, diagnosis, and treatment of primary focal hyperhidrosis. J Am Acad Dermatol. 2004; 51:274-86. [PubMed 15280848]



8. Solish N, Bertucci V, Dansereau A et al. A comprehensive approach to the recognition, diagnosis, and severity-based treatment of focal hyperhidrosis: recommendations of the Canadian hyperhidrosis advisory committee. Dermatol Surg. 2007; 33:908-23. [PubMed 17661933]



9. Stolman LP. Treatment of hyperhidrosis. Dermatol Clin. 1998; 16:863-9. [PubMed 9891696]



10. Haider A, Solish N. Focal hyperhidrosis: diagnosis and management. CMAJ. 2005; 172:69-75. [PubMed 15632408]



11. International Hyperhidrosis Society. Hyperhidrosis treatments, antiperspirants. From the IHS Website (www.sweathelp.org/English/PFF_Treatment_Antiperspirants.asp). Accessed January 14, 2008.



12. Hölzle E, Braun-Falco O. Structural changes in axillary eccrine glands following long-term treatment with aluminum chloride hexahydrate solution. Br J Dermatol. 1984; 110:399-403.



13. Tögel B, Greve B, Raulin C. Current therapeutic strategies for hyperhidrosis: a review. Eur J Dermatol. 2002; 12:219-23.



14. Connolly M, de Berker D. Management of primary hyperhidrosis, a summary of the different treatment modalities. Am J Clin Dermatol. 2003; 4:681-97. [PubMed 14507230]



15. DSE Healthcare Solutions, LLC. Certain Dri (aluminum chloride) anti-perspirant patient information. Edison, NJ; 2006 Mar.



16. Food and Drug Administration. Antiperspirant drug products for over-the-counter human use; final monograph. 21 CFR Parts 310, 350 and 369. Final Rule. [Docket No. 78N-0064] Fed Regist. 2003; 68:34273-93.



17. Guillard O, Fauconneau B, Olichon D et al. Hyperaluminemia in a woman using an aluminum-containing antiperspirant for 4 years. Am J Med. 2004; 117:956-9. [PubMed 15629736]



More Aluminum Chloride Hexahydrate topical resources


  • Aluminum Chloride Hexahydrate topical Side Effects (in more detail)
  • Aluminum Chloride Hexahydrate topical Use in Pregnancy & Breastfeeding
  • Aluminum Chloride Hexahydrate topical Support Group
  • 162 Reviews for Aluminum Chloride Hexahydrate - Add your own review/rating


  • Drysol Solution MedFacts Consumer Leaflet (Wolters Kluwer)

  • Drysol topical Concise Consumer Information (Cerner Multum)

  • Hypercare Prescribing Information (FDA)



Compare Aluminum Chloride Hexahydrate topical with other medications


  • Hyperhidrosis

Monday, 19 March 2012

lovastatin



loe-va-STAT-in


Commonly used brand name(s)

In the U.S.


  • Altoprev

  • Mevacor

Available Dosage Forms:


  • Tablet

  • Tablet, Extended Release

Therapeutic Class: Antihyperlipidemic


Pharmacologic Class: HMG-COA Reductase Inhibitor


Uses For lovastatin


Lovastatin is used together with a proper diet to treat high cholesterol levels in the blood. Using lovastatin may help prevent medical problems caused by such substances clogging the blood vessels. lovastatin may also be used to prevent certain types of heart problems in patients with risk factors for heart problems .


Lovastatin belongs to the group of medicines called 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors. It works by blocking an enzyme that is needed by the body to make cholesterol, thereby reducing the amount of cholesterol in the blood .


Lovastatin is available only with your doctor's prescription .


Importance of Diet


Before prescribing medicine for your condition, your doctor will probably try to control your condition by prescribing a personal diet for you. Such a diet may be low in fats, sugars, and/or cholesterol. Many people are able to control their condition by carefully following their doctor's orders for proper diet and exercise. Medicine is prescribed only when additional help is needed and is effective only when a schedule of diet and exercise is properly followed .


Lovastatin should not be taken with large amounts of grapefruit juice or other grapefruit products because these may increase the concentrations of lovastatin in the body .


Before Using lovastatin


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For lovastatin, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to lovastatin or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatrics-specific problems that would limit the usefulness of lovastatin regular tablets for children aged 10 to 17 years. However, safety and efficacy in children younger than 10 years of age have not been established .


Adolescent girls taking lovastatin regular tablets should be counseled on appropriate contraceptive methods to prevent pregnancy .


Appropriate studies have not been performed on the relationship of age to the effects of lovastatin extended-release tablets in patients younger than 20 years of age. Safety and efficacy have not been established .


Geriatric


Appropriate studies performed to date have not demonstrated geriatrics-specific problems that would limit the usefulness of lovastatin in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require an adjustment in the dose for patients receiving lovastatin extended-release tablets .


Pregnancy








Pregnancy CategoryExplanation
All TrimestersXStudies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities. This drug should not be used in women who are or may become pregnant because the risk clearly outweighs any possible benefit.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking lovastatin, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using lovastatin with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Atazanavir

  • Boceprevir

  • Clarithromycin

  • Darunavir

  • Fosamprenavir

  • Itraconazole

  • Lopinavir

  • Mibefradil

  • Ritonavir

  • Saquinavir

  • Telaprevir

  • Tipranavir

Using lovastatin with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Amiodarone

  • Amprenavir

  • Bezafibrate

  • Ciprofibrate

  • Clofibrate

  • Colchicine

  • Conivaptan

  • Cyclosporine

  • Dalfopristin

  • Danazol

  • Daptomycin

  • Delavirdine

  • Erythromycin

  • Everolimus

  • Fenofibrate

  • Fluconazole

  • Gemfibrozil

  • Indinavir

  • Ketoconazole

  • Nefazodone

  • Nelfinavir

  • Niacin

  • Posaconazole

  • Quinupristin

  • Ranolazine

  • Telithromycin

  • Verapamil

Using lovastatin with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Azithromycin

  • Bosentan

  • Diltiazem

  • Oat Bran

  • Pectin

  • St John's Wort

  • Voriconazole

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using lovastatin with any of the following may cause an increased risk of certain side effects but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use lovastatin, or give you special instructions about the use of food, alcohol, or tobacco.


  • Grapefruit Juice

Other Medical Problems


The presence of other medical problems may affect the use of lovastatin. Make sure you tell your doctor if you have any other medical problems, especially:


  • Alcohol abuse (or history of) or

  • Liver disease, history—Use with caution. These conditions may increase the amount of lovastatin in your blood .

  • Diabetes mellitus, uncontrolled - Use with caution.

  • Kidney disease, severe—Use with caution. lovastatin may make the condition worse .

  • Liver disease, active or

  • Liver enzymes, persistently high levels—lovastatin should NOT be used in these conditions. Use of lovastatin may make liver problems worse .

Proper Use of lovastatin


Take lovastatin only as directed by your doctor. Do not take more or less of it, and do not take more or less often than your doctor ordered .


Follow carefully the special diet your doctor gave you. This is the most important part of controlling your condition and is necessary if the medicine is to work properly .


Remember that lovastatin will not cure your condition, but it does help control it. You must continue to take it as directed if you expect to keep your cholesterol levels down .


Swallow the whole. Do not crush, break, or chew it .


Dosing


The dose of lovastatin will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of lovastatin. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For high cholesterol:
    • For oral dosage form (tablets):
      • Adults—At first, 20 milligrams (mg) once daily given with the evening meal. Your doctor may increase your dose up to a maximum of 80 mg per day if needed.

      • Children (10 to 17 years of age)—At first, 10 milligrams (mg) once daily given with the evening meal. Your doctor may increase your dose up to a maximum of 40 mg per day if needed.

      • Children (less than 10 years of age)—Use and dose must be determined by your doctor .


    • For oral dosage form (extended-release tablets):
      • Adults—At first, 20 milligrams (mg) once a day in the evening at bedtime. Your doctor may increase your dose, but the dose is usually not more than 60 mg once a day.

      • Children—Use and dose must be determined by your doctor .



Missed Dose


If you miss a dose of lovastatin, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using lovastatin


It is very important that your doctor check your progress at regular visits to make sure that lovastatin is working properly. Blood tests may be needed to check for unwanted effects .


Your doctor will need to check your liver before you start using lovastatin .


Check with your doctor immediately if you think that you may be pregnant. Do not take lovastatin if you are pregnant. lovastatin may cause birth defects or other problems in the baby if taken during pregnancy. Do not breastfeed while you are using lovastatin .


Before having any kind of surgery (including dental surgery) or emergency treatment, tell the medical doctor or dentist in charge that you are taking lovastatin .


Do not use excessive amounts of alcohol while taking lovastatin because it can worsen the adverse effects of lovastatin on the liver .


Check with your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness, especially if it is accompanied by unusual tiredness or fever. These may be symptoms of a muscle condition called rhabdomyolysis, which can lead to serious kidney problems .


Do not take other medicines unless thy have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements .


lovastatin Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


Less common
  • Bladder pain

  • bloody or cloudy urine

  • chest tightness

  • cough

  • dark-colored urine

  • difficult, burning, or painful urination

  • difficulty with moving

  • fever

  • frequent urge to urinate

  • headache

  • joint pain

  • lower back or side pain

  • muscle aching, cramps, spasms, or stiffness

  • muscle pain, tenderness, or weakness

  • pain or tenderness around the eyes and cheekbones

  • shortness of breath

  • stuffy or runny nose

  • swollen joints

  • trouble with breathing

  • unusual tiredness or weakness

  • wheezing

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Less common
  • Acid or sour stomach

  • belching

  • bloated, full feeling

  • blurred vision

  • diarrhea

  • difficulty having a bowel movement (stool)

  • dizziness

  • excess air or gas in the stomach or intestines

  • heartburn

  • indigestion

  • lack or loss of strength

  • nausea

  • passing gas

  • rash

  • stomach discomfort, upset, or pain

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: lovastatin side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More lovastatin resources


  • Lovastatin Side Effects (in more detail)
  • Lovastatin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Lovastatin Drug Interactions
  • Lovastatin Support Group
  • 6 Reviews for Lovastatin - Add your own review/rating


  • Lovastatin Prescribing Information (FDA)

  • Lovastatin Professional Patient Advice (Wolters Kluwer)

  • Lovastatin Monograph (AHFS DI)

  • Lovastatin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Altocor Consumer Overview

  • Altoprev Extended-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Altoprev Prescribing Information (FDA)

  • Mevacor Prescribing Information (FDA)



Compare lovastatin with other medications


  • High Cholesterol
  • High Cholesterol, Familial Heterozygous
  • Hyperlipoproteinemia
  • Hyperlipoproteinemia Type IIa, Elevated LDL
  • Hyperlipoproteinemia Type IIb, Elevated LDL VLDL

Saturday, 17 March 2012

femhrt HRT


Generic Name: ethinyl estradiol and norethindrone (HRT) (ETH in ill ess tra DYE ole/ nor ETH in drone)

Brand Names: femhrt, femhrt 1 mg/5 mcg


What are ethinyl estradiol and norethindrone?

Ethinyl estradiol is a form of estrogen. Estrogen is a female sex hormone necessary for many processes in the body.


Norethindrone is a form of progesterone. Progesterone is a female hormone important for the regulation of ovulation and menstruation.


The combination of ethinyl estradiol and norethindrone is used to treat symptoms of menopause such as hot flashes, and vaginal dryness, burning, and irritation. It is also used to prevent osteoporosis.


Estradiol and norethindrone may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about ethinyl estradiol and norethindrone?


This medication can cause birth defects. Do not use if you are pregnant. Tell your doctor right away if you become pregnant, or if you miss two menstrual periods in a row. Do not use this medication if you have any of the following conditions: a history of stroke or blood clot, circulation problems, a hormone-related cancer such as breast or uterine cancer, abnormal vaginal bleeding, if you have recently had a stroke or heart attack, if you have had your uterus removed (hysterectomy), or if you have ever had an allergic reaction to birth control pills or other hormones.

Before taking ethinyl estradiol and norethindrone, tell your doctor if you have high blood pressure or heart disease, high cholesterol, gallbladder disease, diabetes, asthma, seizures, liver disease, a thyroid disorder, high levels of calcium in your blood, migraine headaches or a history of depression, fibroid tumors in your uterus, or a history of breast cancer or an abnormal mammogram.


Avoid smoking while using this medication. Smoking can increase your risk of blood clots, stroke, or heart attack caused by taking hormones.

Have regular physical exams and self-examine your breasts for lumps on a monthly basis while using ethinyl estradiol and norethindrone.


What should I discuss with my healthcare provider before taking ethinyl estradiol and norethindrone?


This medication can cause birth defects. Do not use if you are pregnant. Tell your doctor right away if you become pregnant, or if you miss two menstrual periods in a row. Do not use this medication if you have:

  • abnormal vaginal bleeding that a doctor has not checked;




  • a hormone-related cancer such as breast or uterine cancer;




  • a history of blood clot or circulation problems;




  • if you have recently had a stroke or heart attack;




  • if you have had your uterus removed (hysterectomy); or




  • if you have ever had an allergic reaction to birth control pills or other hormones.



Before using this medication, tell your doctor if you have any of the following conditions.



  • high blood pressure or heart disease;




  • high cholesterol, gallbladder disease, or diabetes;




  • asthma;




  • epilepsy or other seizure disorder;




  • liver disease;




  • a thyroid disorder;




  • high levels of calcium in your blood;




  • migraine headaches or a history of depression;




  • fibroid tumors in your uterus; or




  • a history of breast cancer or an abnormal mammogram.



If you have any of these conditions, you may need a dose adjustment or special tests to safely use this medication.


The hormones in this medication can pass into breast milk and may harm a nursing baby. This medication may also slow breast milk production. Do not use if you are breast-feeding a baby.

How should I take ethinyl estradiol and norethindrone?


Use this medication exactly as it was prescribed for you. Do not use the medication in larger amounts, or use it for longer than recommended by your doctor. Follow the instructions on your prescription label.


Try to take your medicine at the same time each day.


If you need to have any type of medical tests or surgery, or if you will be on bed rest, you may need to stop using this medication for a short time. Any doctor or surgeon who treats you should know that you are using hormones.


It is important to use ethinyl estradiol and norethindrone regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.


Have regular physical exams and self-examine your breasts for lumps on a monthly basis while using ethinyl estradiol and norethindrone.


Store this medication at room temperature away from moisture and heat.

See also: Femhrt dosage (in more detail)

What happens if I miss a dose?


Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the dose you missed and take only the next regularly scheduled dose. Do not take a double dose of this medication.


What happens if I overdose?


An overdose of ethinyl estradiol and norethindrone is unlikely to threaten life. Call an emergency room or poison control center for advice.

Symptoms of a ethinyl estradiol and norethindrone overdose might include nausea, vomiting, and vaginal bleeding.


What should I avoid while taking my ethinyl estradiol and norethindrone?


Follow your doctor's instructions about any restrictions on food, beverages, or activity while you are using this medication.


Avoid smoking while using this medication. Smoking can increase your risk of blood clots, stroke, or heart attack caused by taking hormones.

My ethinyl estradiol and norethindrone side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medication and call your doctor at once if you have any of these serious side effects:

  • sudden numbness or weakness, especially on one side of the body;




  • sudden headache, confusion, pain behind the eyes, problems with vision, speech, or balance;




  • chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling; or




  • gallbladder problems (pain in your upper right stomach area with nausea and vomiting);




  • jaundice (yellowing of the skin or eyes); or




  • a breast lump.



Less serious side effects may include:



  • mild nausea, vomiting, stomach pain;




  • breast tenderness or swelling;




  • freckles or darkening of facial skin;




  • increased hair growth, loss of scalp hair;




  • changes in weight or appetite;




  • problems with contact lenses;




  • runny nose;




  • vaginal itching or discharge;




  • changes in your menstrual periods, decreased sex drive; or




  • headache, dizziness, sleep problems.



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect ethinyl estradiol and norethindrone?


Before taking ethinyl estradiol and norethindrone, tell your doctor if you are taking any of the following medicines:



  • acetaminophen (Tylenol);




  • cyclosporine (Neoral, Gengraf, Sandimmune);




  • prednisolone (Orapred);




  • theophylline (Respbid, Theo-Dur);




  • St. John's wort;




  • an antibiotic such as clarithromycin (Biaxin), erythromycin (E.E.S., E-Mycin, Ery-Tab, Erythrocin), itraconazole (Sporanox), or ketoconazole (Nizoral);




  • seizure medication such as carbamazepine (Carbatrol, Tegretol) or phenobarbital (Solfoton);




  • rifampin (Rifadin, Rifamate, Rimactane); or




  • HIV or AIDS medication such as ritonavir (Norvir, Kaletra).



This list is not complete and there may be other drugs that can interact with ethinyl estradiol and norethindrone. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More femhrt resources


  • Femhrt Side Effects (in more detail)
  • Femhrt Dosage
  • Femhrt Use in Pregnancy & Breastfeeding
  • Drug Images
  • Femhrt Drug Interactions
  • Femhrt Support Group
  • 5 Reviews for Femhrt - Add your own review/rating


Compare femhrt with other medications


  • Abnormal Uterine Bleeding
  • Acne
  • Birth Control
  • Endometriosis
  • Gonadotropin Inhibition
  • Menstrual Disorders
  • Polycystic Ovary Syndrome
  • Postmenopausal Symptoms
  • Prevention of Osteoporosis


Where can I get more information?


  • Your pharmacist can provide more information about ethinyl estradiol and norethindrone.

See also: femhrt side effects (in more detail)


Josamicina




Josamicina may be available in the countries listed below.


Ingredient matches for Josamicina



Josamycin

Josamicina (DCIT) is also known as Josamycin (Rec.INN)

International Drug Name Search

Glossary

DCITDenominazione Comune Italiana
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Friday, 16 March 2012

Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine


Pronunciation: a-seet-a-MIN-oh-fen/dye-FEN-hye-dra-meen/dex-troe-meth-OR-fan/sue-doe-eh-FED-rin
Generic Name: Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine
Brand Name: Night-Time


Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine is used for:

Relieving symptoms of pain, sinus congestion, runny nose, sneezing, and cough due to colds, upper respiratory infections, and allergies. It may also used for other conditions as determined by your doctor.


Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine is a decongestant, antihistamine, cough suppressant and analgesic combination. The decongestant works by constricting blood vessels and reducing swelling in the nasal passages. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The analgesic and cough suppressant work in the brain to decrease pain and to reduce a dry or unproductive cough.


Do NOT use Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine if:


  • you are allergic to any ingredient in Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine

  • you have severe high blood pressure, severe heart blood vessel disease, rapid heartbeat, or severe heart problems

  • you are unable to urinate or are having an asthma attack

  • you take sodium oxybate (GHB) or have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.



Before using Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine:


Some medical conditions may interact with Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have a fast, slow, or irregular heartbeat

  • if you have a history of adrenal gland problems (eg, adrenal gland tumor); heart problems; high blood pressure; diabetes; heart blood vessel problems; stroke; glaucoma; a blockage of your stomach, bladder, or intestines; ulcers; trouble urinating; an enlarged prostate or other prostate problems; seizures; overactive thyroid; or liver problems; severe kidney problems; or if you consume more than 3 alcohol-containing drinks per day

  • if you have a history of asthma, chronic cough, lung problems (eg, chronic bronchitis, emphysema), or chronic obstructive pulmonary disease (COPD), or if your cough occurs with large amounts of mucus

Some MEDICINES MAY INTERACT with Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Beta-blockers (eg, propranolol), catechol-O-methyltransferase (COMT) inhibitors (eg, tolcapone), furazolidone, indomethacin, isoniazid, MAO inhibitors (eg, phenelzine), sodium oxybate (GHB), or tricyclic antidepressants (eg, amitriptyline) because side effects of Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may be increased

  • Anticoagulants (eg, warfarin), digoxin or droxidopa because risk of bleeding, irregular heartbeat or heart attack may be increased

  • Bromocriptine or hydantoins (eg, phenytoin) because side effects may be increased by Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine

  • Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because effectiveness may be decreased by Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine

This may not be a complete list of all interactions that may occur. Ask your health care provider if Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine:


Use Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may be taken with or without food.

  • If you miss a dose of Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine.



Important safety information:


  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may cause dizziness, drowsiness, or blurred vision. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine. Using Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.

  • Do not take diet or appetite control medicines while you are taking Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine without checking with you doctor.

  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine contains acetaminophen, diphenhydramine, dextromethorphan, and pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains acetaminophen, diphenhydramine, dextromethorphan, or pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist.

  • Do NOT exceed the recommended dose or take Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine for longer than prescribed without checking with your doctor.

  • If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor.

  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may cause liver damage. If you consume 3 or more alcohol-containing drinks every day, ask your doctor if you should take Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine or other pain relievers/fever reducers. Alcohol use combined with Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine may increase your risk for liver damage.

  • If you are scheduled for allergy skin testing, do not take Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine for several days before the test because it may decrease your response to the skin tests.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine.

  • Use Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine with caution in the ELDERLY because they may be more sensitive to its effects.

  • Caution is advised when using Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine in CHILDREN because they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine, discuss with your doctor the benefits and risks of using Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine during pregnancy. It is unknown if Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine is excreted in breast milk. Do not breast-feed while taking Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine.


Possible side effects of Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; diarrhea; dizziness; drowsiness; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; stomach pain; tremor; trouble sleeping; vision changes; yellowing of skin or eyes.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.


Proper storage of Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine:

Store Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine out of the reach of children and away from pets.


General information:


  • If you have any questions about Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine, please talk with your doctor, pharmacist, or other health care provider.

  • Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Acetaminophen/Diphenhydramine/Dextromethorphan/Pseudoephedrine resources


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Monday, 12 March 2012

All Day Allergy Drug Facts





Dosage Form: tablet
McKesson All Day Allergy Drug Facts

Active ingredient (in each tablet)


Cetirizine HCl 10 mg



Purpose


Antihistamine



Uses


temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:


  • runny nose

  • sneezing

  • itchy, watery eyes

  • itching of the nose or throat


Warnings



Do not use


if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.



Ask a doctor before use if you have


liver or kidney disease. Your doctor should determine if you need a different dose.



Ask a doctor or pharmacist before use if you are


taking tranquilizers or sedatives.



When using this product


  • drowsiness may occur

  • avoid alcoholic drinks

  • alcohol, sedatives, and tranquilizers may increase drowsiness

  • be careful when driving a motor vehicle or operating machinery


Stop use and ask a doctor if


an allergic reaction to this product occurs. Seek medical help right away.



If pregnant or breast-feeding:


  • if breast-feeding: not recommended

  • if pregnant: ask a health professional before use.


Keep out of reach of children.


In case of overdose, get medical help or contact a Poison Control Center right away.



Directions












adults and children


6 years and over
one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and overask a doctor
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information


  • do not use if blister unit is broken or torn

  • store between 20° to 25°C (68° to 77°F)


Inactive ingredients


corn starch, FD&C blue no. 1, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin



Questions or comments?


1-800-719-9260



Principal Display Panel


Compare to Zyrtec® active ingredient


24 Hour


All Day Allergy


Cetirizine Hydrochloride Tablets, 10 mg


Antihistamine


Indoor & Outdoor Allergies


24 Hour Relief of sneezing, runny nose, itchy, watery eyes, itchy throat or nose


Original Prescription Strength


Allergy


Actual Size


All Day Allergy Carton










SUN MARK ALL DAY ALLERGY  24 HOUR
cetirizine hydrochloride  tablet










Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)49348-847
Route of AdministrationORALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (CETIRIZINE)CETIRIZINE HYDROCHLORIDE10 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize10mm
FlavorImprint Code4H2
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
149348-847-461 BLISTER PACK In 1 CARTONcontains a BLISTER PACK
114 TABLET In 1 BLISTER PACKThis package is contained within the CARTON (49348-847-46)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07833601/21/2008


Labeler - McKesson (177667227)
Revised: 05/2009McKesson




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