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Europaisches Patent amt European Patent Office European DES brevets EUROPEAN00 Publication number:PATENT Date of publication of patent specification: 07.08.910157695B1SPECIFICATION Int. Cl.5: A61K9/22
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Step 1: Start by reading the instructions and understanding the dose of the controlled release solid drug.
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Step 2: Wash your hands thoroughly with soap and water to maintain cleanliness.
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Step 3: Take the controlled release solid drug with a full glass of water, unless otherwise directed by your healthcare provider.
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Step 4: Swallow the tablet or capsule whole without crushing, breaking, or chewing it.
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What is controlled release solid drug?
Controlled release solid drugs are medications that are designed to release the active ingredient slowly over a period of time.
Who is required to file controlled release solid drug?
Manufacturers and distributors of controlled release solid drugs are required to file with the appropriate regulatory authorities.
How to fill out controlled release solid drug?
To fill out a controlled release solid drug, manufacturers must provide detailed information about the drug's formulation, release mechanism, and intended use.
What is the purpose of controlled release solid drug?
The purpose of controlled release solid drugs is to maintain a steady level of medication in the body over an extended period of time, leading to longer-lasting effects and reduced side effects.
What information must be reported on controlled release solid drug?
Information that must be reported on controlled release solid drugs includes the active ingredient, dosage strength, release profile, and any potential side effects.
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