Buy Sandomigran DS from Canadian & International Pharmacies
Sandomigran DS (Pizotifen Malate)and/or alternatives
Sandomigran DS 1mg from $1.04 USD/tabletSandomigran DS 1mg
Manufactured by: Paladin Labs Inc.
Product of Canada. Shipped from CanadaRxPrescription Required
General Information on Sandomigran DS
Sandomigran DS is used to treat patients suffering from migraine headaches. This medicine affects the neurotransmitters in the patient’s brain. The generic name of this drug is Pizotifen. Its inactive ingredients are lactose, magnesium stearate and microcrystalline cellulose. This drug is available as Sandomigran DS 1 mg tablet.
You can only buy Sandomigran DS as per a doctor’s prescription.
Side effects of Sandomigran DS
You should not buy Sandomigran DS online if :
- You have hypersensitivity to Pizotifen or any of the ingredients of the medication
- You are taking monoamine oxidase (MAO) inhibitors such as tranylcypromine or phenelzine
Before you buy Sandomigran DS, inform your doctor if you have any of the following:
- Less than 12 years of age
- A pyloroduodenal obstruction or stenosing pyloric ulcer
- Narrow-angle glaucoma
- Urinary retention
- Heart disease
- Reduced liver or kidney function
- Drowsiness or reduced alterness
Some of the common, and mild, side effects of this drug are:
- Erectile dysfunction
- Increased appetite
You should consult your doctor immediately if your experience any of the following side effects:
- Severe allergic reaction symptoms such as hives, difficulty breathing, swelling of the mouth or throat
- Low blood pressure
- Muscle pain
- Swelling of legs or feet
- Vision changes
Pregnant women should take Sandomigran DS only if their doctor has prescribed it. Nursing mothers should avoid this drug since it passes into breast milk and could harm a nursing baby.
Dosage of Sandomigran DS
A patient should start a dose as low as 0.5mg Sandomigran DS 1mg three times a day and gradually increase it to 0.5 mg Sandomigran DS 1 mg tablet three times a day. The average maintenance dose is 1.5gm Sandomigran DS 1 mg. Factors that could affect the medication dose prescribed include body weight, other medications and other medical conditions.
The recommended dosage ranges from 1mg Sandomigran DS 1mg to 6mg Sandomigran DS 1mg a day, depending upon response of the patient to medication. The dosage has to gradually reduce in order to prevent a rebound headache. It may take up to a month for this medication to show its maximum effect in a patient.
It is important for a patient to take this medication as prescribed by a doctor. However, if a patient misses a dose, he or she should take a missed dose as soon as possible. You can continue with your regular schedule if it is already time for your next dose of this medicine. A patient should avoid taking two doses at a time. In case of an overdose, a patient should immediately take assistance of a healthcare provider.
There are many drugs that could interact with Sandomigran DS. These include alcohol, barbiturates such as Phenobarbital, butalbital, benzodiazepines such as diazepam, Iorazepam, betahistine, cholinesterase inhibitors such as donepezil, galantamine, rivastigmine, droperidol, anticholinergic medications such as benztropine, diphenhydramine, oxybutynin, phenothiazines such as perphenazine, thioridazine, sedatives, pramlintide, sleeping pills and tricyclic antidepressants such as amitriptyline and desipramine.
A patient should inform doctor if he or she is taking other over-the-counter medicines, herbal medications or supplements since alcohol, caffeine or street drugs can affect the action of Sandomigran DS.
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What is a "Generic" medication/drug?
Generic drugs are medications that have the comparable medicinal ingredients as the original brand name drug, but which are generally cheaper in price. Nearly 1 in 3 drugs dispensed are "generic". They undergo comparative testing to ensure that they are the same as their "brand" counterparts in:
- Active Ingredient (e.g. "Pravastatin" is the active ingredient in brand name Pravachol)
- Dosage (e.g. 10 mg of the active ingredient)
- Safety (e.g. same or similar side effects, drug interactions)
- Performance (e.g. 10 mg of a "generic" can be substituted for 10 mg of the "brand" and have the same therapeutic result)
- Intended use (e.g. both "generic" and "brand" would be prescribed for the same conditions)
What this means is that "generic" medications can be used as a substitute of their brand equivalents with comparable therapeutic results. There are a few exceptions (examples are outlined at the end of this page) and as always you should consult your physician before switching from a brand name medications to a generic or vice versa.
What differences are there between generic and brand?
While generics and brand equivalent drugs contain comparable active ingredients, they may be different in the following ways:
- Appearance (e.g. the scoring or markings)
The color, shape and size of the medication come from the fillers that are added to the active ingredients to make the drug. These fillers that are added to the drug have no medical use and do not to change the effectiveness of the final product. A generic drug must contain comparable active ingredients and must be comparable in strength and dosage to the original brand name equivalent. Generic drugs can be more cost effective than purchasing the brand name.
Why do generics cost less than the brand name equivalents?
When a new drug is "invented", the company that discovered it has a patent on it that gives them the exclusive production rights for this medication. Once the patent expires in a country, other companies can bring the product to market under their own name. This patent prevents other companies from copying the drug during that time so they can earn back their Research and Development costs through being the exclusive supplier of the product. After the patent expires however, other companies can develop a "generic" version of the product. These versions generally are offered at much lower prices because the companies do not have the same development costs as the original company who developed the medication.
The main thing to realize here though is that the two products are therapeutically comparable. They may look different, and be called something different, but they are required to be have the same active ingredient.
How are Generic drugs tested to ensure quality and efficacy?
The two most generally accepted methods to prove the safety of a generic version of a drug are to either repeat most of the chemistry, animal and human studies originally done, or to show that the drug performs comparably with the original brand name drug. This second option is called a "comparative bioavailability" study. During this type of study, volunteers are given the original drug, and then separately later the generic drug. The rates at which the drug is delivered to the patient (into their blood stream or otherwise absorbed) are measured to ensure they are the same. Because the same active ingredient is used the major concern is just that it delivers the common chemical(s) at the same rate so that they have the same effect. Please note that the methods that the manufacturers use may vary from country to country.