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Ocu-Sul 30

Generic Name: sulfacetamide ophthalmic (SUL fa SEET a mide off THAL mik)
Brand Names: Bleph-10, Ocu-Sul 10, Ocu-Sul 15, Ocu-Sul 30, Sodium Sulamyd, Sulf-10, Sulfac 10%

What is Ocu-Sul 30 (sulfacetamide ophthalmic)?

Sulfacetamide ophthalmic is an antibiotic.

Sulfacetamide ophthalmic is used to treat bacterial infections of the eyes.

Sulfacetamide ophthalmic may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Ocu-Sul 30 (sulfacetamide ophthalmic)?

Do not touch the dropper or tube opening to any surface, including your eyes or hands. The dropper or tube opening is sterile. If it becomes contaminated, it could cause an infection in your eye.

Apply light pressure to the inside corner of your eye (near your nose) after each drop to prevent the fluid from draining down your tear ducts.

Who should not use Ocu-Sul 30 (sulfacetamide ophthalmic)?

Do not use sulfacetamide ophthalmic if you have a viral or fungal infection in your eye. It is used to treat infections caused by bacteria only.

Do not use sulfacetamide ophthalmic if you have ever had an allergic reaction to a sulfa-based drug.

It is not known whether sulfacetamide ophthalmic will harm an unborn baby. Do not use sulfacetamide ophthalmic without first talking to your doctor if you are pregnant. It is also not known whether sulfacetamide ophthalmic passes into breast milk. Do not use sulfacetamide ophthalmic without first talking to your doctor if you are breast-feeding a baby.

How should I use Ocu-Sul 30 (sulfacetamide ophthalmic)?

Use sulfacetamide ophthalmic eyedrops or ointment exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Wash your hands before using your ey


Polymyxin B Sulfate topical

Class: Polymyxins
VA Class: AM900
CAS Number: 1405-20-5
Brands: Poly-Rx, Neosporin G.U. Irrigant

  • Administer IV, IM, or intrathecally only to hospitalized patients under constant supervision by a clinician.100 101 102

  • Nephrotoxic.100 101 102 Assess renal function prior to therapy.100 101 102 Reduce dosage in patients with renal damage and nitrogen retention.100 101 102 Polymyxin B-associated nephrotoxicity usually manifests as albuminuria, cellular casts, and azotemia.100 101 102 Discontinue in patients with decreasing urine output and increasing BUN.100 101 102

  • Neurotoxic.100 101 102 Neurotoxicity may be manifested by irritability, weakness, drowsiness, ataxia, perioral paresthesia, numbness of the extremities, and vision blurring.100 101 102 Usually associated with high polymyxin B serum concentrations found in patients with impaired renal function and/or nephrotoxicity.100 101 102


carbetocin Intravenous

kar-be-TOE-sin

Available Dosage Forms:

  • Solution

Uses For carbetocin

Carbetocinis a hormone used to control bleeding after delivery.

Carbetocin is available only with your doctor's prescription.

Before Using carbetocin

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 carbetocin, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to carbetocin 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.

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. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.

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. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.

Other Medical Prob


Levulan Kerastick Topical

Generic Name: aminolevulinic acid (Topical route)

a-mee-noe-lev-ue-LIN-ik AS-id

Commonly used brand name(s)

In the U.S.

  • Levulan Kerastick

Available Dosage Forms:

  • Kit
  • Stick
  • Solution

Therapeutic Class: Photosensitizing Agent

Uses For Levulan Kerastick

Aminolevulinic acid application followed by exposure to a certain type of light (blue light using the BLU–U Blue Light Photodynamic Therapy Illuminator) treats the skin condition called actinic keratoses.

This medicine is available only with your doctor's prescription.

Before Using Levulan Kerastick

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 this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine 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

Studies on this medicine have been done only in adult patients, and there is no specific information comparing use of aminolevulinic acid in children with use in other age groups.

Geriatric

Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults or if they cause different side effects or problems in older people. There is no specific information comparing use of aminolevulinic acid in the elderly with use in other age groups.

Pregnancy

Pregnancy Category Expla


lindane Topical

LIN-dane

Topical route(Lotion;Shampoo)

Lindane should only be used in patients who cannot tolerate or have failed first-line treatment with safer medications for the treatment of scabies. Seizures and deaths have been reported following lindane use. Risk of serious neurotoxicity when used in infants, children, the elderly, individuals with other skin conditions (eg, atopic dermatitis, psoriasis), and in those who weigh less than 110 lbs (50 kg). Lindane is contraindicated in premature infants and individuals with known uncontrolled seizure disorders. Instruct patients on the proper use of lindane .

Commonly used brand name(s)

In the U.S.

  • Kwell
  • Thionex

In Canada

  • Kwellada Lotion 1%
  • Lindane
  • Pms-Lindane

Available Dosage Forms:

  • Cream
  • Shampoo
  • Lotion

Therapeutic Class: Scabicide

Uses For lindane

Lindane , formerly known as gamma benzene hexachloride, is an insecticide and is used to treat scabies and lice infestations.

Lindane cream and lotion are usually used to treat only scabies infestation. Lindane shampoo is used to treat only lice infestations.

Lindane is available only with your doctor's prescription.

Before Using lindane

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 lindane, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to lindane 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 caref


Lustra Cream


Dosage Form: cream
LUSTRA®

LUSTRA®

(HYDROQUINONE CREAM USP, 4%)

The Complete Treatment for Dyschromia

LUSTRA-AF®

(HYDROQUINONE CREAM USP, 4%)

The Complete Treatment for Dyschromia

Rx Only

FOR EXTERNAL USE ONLY

I. DESCRIPTION

Hydroquinone is 1,4-benzenediol. Hydroquinone is structurally related to monobenzone. Hydroquinone occurs as fine, white needles. The drug is freely soluble in water and in alcohol and has a pKa of 9.96. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; molecular weight 110.1. The structural formula is:

C6H6O2

CONTENTS

ACTIVE INGREDIENT

Hydroquinone USP 4%.

OTHER INGREDIENTS (LUSTRA®)

Alcohol, benzyl alcohol, butylated hydroxytoluene, carbomer 940, cetearyl alcohol (and) ceteareth-20, cetyl alcohol, cyclopentasiloxane (and) polysilicone-11, dimethiconol, disodium EDTA, fragrance, glycerin, glyceryl stearate (and) PEG-100 stearate, glycolic acid, hydrogenated lecithin, linoleic acid, magnesium 1-ascorbyl phosphate, phenoxyethanol, phenyl trimethicone, polyacrylamide (and) C13-14 isoparaffin (and) laureth 7, purified water, sodium metabisulfite, sodium citrate dihydrate, vitamin E acetate, vitamin E alcohol, triethanolamine.

OTHER INGREDIENTS (LUSTRA-AF®)

Alcohol, avobenzone, benzyl alcohol, butylated hydroxytoluene, carbomer 940, cetearyl alcohol (and) ceteareth-20, cetyl alcohol, cyclopentasiloxane (and) polysilicone-11, dimethiconol, disodium EDTA, fragrance, glycerin, glyceryl stearate (and) PEG-100 stearate, glycolic acid, hydrogenated lecithin, linoleic acid, magnesium 1-ascorbyl phosph


Dimetapp DM Cold/Cough Elixir

Pronunciation: brome-fen-IR-a-meen/dex-troe-meth-OR-fan/sue-do-eh-FED-rin
Generic Name: Brompheniramine/Dextromethorphan/Pseudoephedrine
Brand Name: Examples include Bromfed DM and Carbodex DM

Dimetapp DM Cold/Cough Elixir is used for:

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

Dimetapp DM Cold/Cough Elixir is a decongestant, antihistamine, and cough suppressant combination. It 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 while the cough suppressant works in the brain to help decrease the cough reflex to reduce a dry cough.

Do NOT use Dimetapp DM Cold/Cough Elixir if:

  • you are allergic to any ingredient in Dimetapp DM Cold/Cough Elixir
  • 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 if you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (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 Dimetapp DM Cold/Cough Elixir:

Some medical conditions may interact with Dimetapp DM Cold/Cough Elixir. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


Curanail 5% w / w Medicated Nail Lacquer

C u r a n a i l

5% w/v Medicated Nail Lacquer

Amorolfine

Curanail 5% w/v Medicated Nail Lacquer

Amorolfine

Read all of this leaflet carefully because it contains important information for you.

This medicine is available without prescription. However, you still need to use Curanail carefully to get the best results from it.

  • Keep this leaflet. You may need to read it again.
  • Ask your pharmacist if you need more information or advice.
  • You must contact a doctor if your symptoms worsen or do not improve within 3 months.
  • If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

In this leaflet:

1. What Curanail is and what it is used for
2. Before you use Curanail
3. How to use Curanail
4. Possible side effects
5. How to store Curanail
6. Further information

What Curanail is and what it is used for

  • Curanail is used to treat fungal infections affecting up to 2 nails and affecting the upper half or sides of the nail (as shown in the first picture below). If the infection appears to be more like pictures 2 or 3, you should consult your doctor.
  • The active substance in Curanail is amorolfine (as the hydrochloride) which belongs to a group of medicines known as antifungals.
  • Amorolfine kills a wide variety of fungi that can cause nail infections. A fungal nail infection is likely to result in discoloured (white, yellow or brown), thick or brittle nails, although their appearance can vary considerably as the following pictures show:


Fluvastatin 20mg Capsules (Winthrop Pharmaceuticals UK Ltd)

1. Name Of The Medicinal Product

Fluvastatin 20mg Capsules

2. Qualitative And Quantitative Composition

One 20mg capsule contains 21.06 mg fluvastatin sodium corresponding to 20 mg fluvastatin.

Excipient:

Each capsule contains 5.00 mg castor oil, hydrogenated

For a full list of excipients, see section 6.1

3. Pharmaceutical Form

Strength 20 mg: white opaque/orange opaque size 3 capsule, hard

4. Clinical Particulars

4.1 Therapeutic Indications

As an adjunct to diet for the reduction of elevated total-C, LDL-C, apo B and TG levels in patients with primary hypercholesterolaemia and mixed dyslipidaemia (Fredrickson types IIa and IIb).

Secondary prevention of coronary events after percutaneous coronary intervention in patients with coronary heart disease. (see section 5.1)

4.2 Posology And Method Of Administration

Prior to treatment, secondary causes of hypercholesterolaemia should be excluded and patients should be placed on a low-cholesterol diet which should be continued during treatment.

Fluvastatin capsules are taken in the evening, independently of food. They should be swallowed whole, not chewed, and taken with some water.

• Hypercholesterolaemia: The recommended starting doses are from 20 to 40 mg, once daily. For those who do not respond to lower dose, the dose may be increased to 40 mg twice daily according to baseline LDL-C levels and therapeutic goals.

• Coronary Heart Disease after percutaneous coronary intervention : The dose is 40 mg twice daily

The maximum recommended daily dose is 80 mg.

Any dose adjustments of fluvastatin should be made at the earliest after 4 weeks, based on the measur


Hidroderm

Hidroderm may be available in the countries listed below.

Ingredient matches for Hidroderm

Urea

Urea is reported as an ingredient of Hidroderm in the following countries:

  • Peru

International Drug Name Search


Panodil Zapp

Panodil Zapp may be available in the countries listed below.

Ingredient matches for Panodil Zapp

Paracetamol

Paracetamol is reported as an ingredient of Panodil Zapp in the following countries:

  • Denmark

International Drug Name Search


Apo-Cefaclor

Apo-Cefaclor may be available in the countries listed below.

Ingredient matches for Apo-Cefaclor

Cefaclor

Cefaclor is reported as an ingredient of Apo-Cefaclor in the following countries:

  • Canada
  • Guyana
  • Vietnam

International Drug Name Search


Citabion

Citabion may be available in the countries listed below.

Ingredient matches for Citabion

Cytarabine

Cytarabine is reported as an ingredient of Citabion in the following countries:

  • Greece

International Drug Name Search


Rebilex-DSR

Rebilex-DSR may be available in the countries listed below.

Ingredient matches for Rebilex-DSR

Domperidone

Domperidone is reported as an ingredient of Rebilex-DSR in the following countries:

  • India
Rabeprazole

Rabeprazole is reported as an ingredient of Rebilex-DSR in the following countries:

  • India

International Drug Name Search


Celeston Chronodose

Celeston Chronodose may be available in the countries listed below.

Ingredient matches for Celeston Chronodose

Betamethasone

Betamethasone 21-acetate (a derivative of Betamethasone) is reported as an ingredient of Celeston Chronodose in the following countries:

  • Luxembourg
  • Norway

International Drug Name Search


Ranitidina Cinfa

Ranitidina Cinfa may be available in the countries listed below.

Ingredient matches for Ranitidina Cinfa

Ranitidine

Ranitidine is reported as an ingredient of Ranitidina Cinfa in the following countries:

  • Portugal

Ranitidine hydrochloride (a derivative of Ranitidine) is reported as an ingredient of Ranitidina Cinfa in the following countries:

  • Dominican Republic
  • El Salvador
  • Guatemala
  • Panama
  • Spain

International Drug Name Search


Fada Difenhidramina

Fada Difenhidramina may be available in the countries listed below.

Ingredient matches for Fada Difenhidramina

Diphenhydramine

Diphenhydramine hydrochloride (a derivative of Diphenhydramine) is reported as an ingredient of Fada Difenhidramina in the following countries:

  • Argentina

International Drug Name Search


Céfotétan

Céfotétan may be available in the countries listed below.

Ingredient matches for Céfotétan

Cefotetan

Céfotétan (DCF) is known as Cefotetan in the US.

International Drug Name Search

Glossary

DCFDénomination Commune Française

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


Calaptin

Calaptin may be available in the countries listed below.

Ingredient matches for Calaptin

Verapamil

Verapamil hydrochloride (a derivative of Verapamil) is reported as an ingredient of Calaptin in the following countries:

  • India

International Drug Name Search


Novodigal

Novodigal may be available in the countries listed below.

Ingredient matches for Novodigal

Acetyldigoxin

Acetyldigoxin ß-isomer (a derivative of Acetyldigoxin) is reported as an ingredient of Novodigal in the following countries:

  • Germany

International Drug Name Search



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