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Generic drugs manufacturers do not need to spend huge amounts on scientific research and development, on extensive clinical trials and marketing campaigns.
The safety and effectiveness of generic drugs are established by the fact that all of them go through the FDA review and approval procedure.
To put it differently generics have identical active ingredients and their pharmacological effects are the same, as those of their brand-name equivalents.





















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Patients will remain at one dose level for one week before escalated to the next higher dose level, providing that no grade II or III toxicity occurs.

Disulfiram blocks the metabolic breakdown of alcohol in a person's system, causing him or her to develop hangover-like symptoms in as little as five minutes after drinking.

Acetaldehyde itself is the cause of many symptoms from alcohol use.

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Antipsychotics have been used since the 1970s when the first report was published on the use of for the treatment of monosymptomatic hypochondriacal psychosis (now classified as a delusional disorder, somatic type by DSM-5).

Manufacturers of generic drugs cannot use brand names on their pharmaceuticals as that would be the breach of copyright while using the well known ingredients is absolutely legal.

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Sulfites, once used to keep fruits and vegetables from turning brown, were banned from many foods by the United States Food and Drug Administration in 1986 due their potential for allergic reactions.

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