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March 20, Investor Faq Get answers to important investor relation questions. IR Contact Get answers to your investor relation questions. Powered By Q4 Inc. To prevent malaria - the recommended adult dose is mg of Hydroxychloroquine on the same day each week. You need to start taking Plaquenil two weeks before visiting an endemic area and continue suppressive therapy for eight weeks after leaving the endemic area. To treat malaria - the recommended initial dose for adults is mg Hydroxychloroquine followed by one mg Hydroxychloroquine dose in the next hours.
You will also be required to take one mg dose each day for the following two consecutive days. To treat lupus erythematosus - the recommended initial dose for adults is mg Hydroxychloroquine once or twice a day. The maintenance dose is in the range of mg to mg daily. To treat rheumatoid arthritis — the recommended initial dose for adults is in the range of mg to mg daily.
The maintenance dose is in the range of mg to mg. Take the Plaquenil mg tablet with food or a glass of milk.
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Plaquenil may potentially interact with other medicines you are using and cause side effects. It may interact with specific beta blockers, specific parasite medications, Digoxin, Mefloquine, Cyclosporine, and Phenothiazines. This is not a complete list of medications that may interact with Plaquenil. Note that not all products are shipped by our contracted Canadian pharmacy. This website contracts with dispensaries around the world that ship products directly to our customers.
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The items within your order may be shipped from any one of these jurisdiction depending on the availability and cost of the products at the time you place your order. The products are sourced from these countries as well as others. Please note that the product appearance may vary from actual product received depending on availability. 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".
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They undergo comparative testing to ensure that they are the same as their "brand" counterparts in:. What this means is that "generic" medications can be used as a substitute of their brand equivalents with comparable therapeutic results.
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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. While generics and brand equivalent drugs contain comparable active ingredients, they may be different in the following ways:. 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. 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.
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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.
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.
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