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DRUG AND DIETARY SUPPLEMENT PROFILES

A comprehensive review of the safety and effectiveness of this drug. If the drug is not a Do Not Use product, information on adverse effects, drug interactions and how to use the medication are included.
Search results below include Drug and Dietary Supplement Profiles where your selected drug is a secondary subject of discussion.

esomeprazole (NEXIUM, NEXIUM 24HR); lansoprazole (PREVACID, PREVACID 24HR); omeprazole (PRILOSEC, PRILOSEC OTC, YOSPRALA); pantoprazole (PROTONIX); rabeprazole (ACIPHEX)
dextroamphetamine (DEXEDRINE); various amphetamines (ADDERALL, ADDERALL XR, ADZENYS, ADZENYS XR-ODT, DYANAVEL XR)
butalbital, acetaminophen and caffeine (ESGIC PLUS, FIORICET); butalbital, caffeine and aspirin (FIORINAL); butalbital, caffeine, aspirin and codeine (FIORINAL WITH CODEINE)
  • We list these drugs as Do Not Use drugs because they are irrational combinations that include drugs that are unsafe or ineffective.

WORST PILLS, BEST PILLS NEWSLETTER ARTICLES

Search results below include Worst Pills, Best Pills Newsletter Articles where your selected drug is a secondary subject of discussion.

SSRIs Can Have Dangerous Interactions With Other Drugs
January 2008
More than 70 million prescriptions a year are filled for these popular antidepressants, including Prozac, Paxil, Zoloft, Luvox, Celexa and Lexapro. This article gives details about more than 60 other widely prescribed prescription drugs that can have harmful interactions if used with these antidepressants. The two different kinds of interactions are also discussed.

ADDITIONAL INFORMATION FROM PUBLIC CITIZEN

Search results below include Additional Information from Public Citizen where your selected drug is a secondary subject of discussion.

Testimony regarding the FDA's categorization of "morning sickness" and "leg edema" during pregnancy as conditions not diseases which allows dietary supplement manufacturers to promote for these symptoms (HRG Publication #1517)
Under the dangerous provisions of DSHEA, that categorization allows dietary supplement manufacturers to promote products as treatments of those conditions without first proving that the products are safe and effective.
Letter to the Food and Drug Administration regarding their final regulations on dietary supplements and their definition of adverse effects of pregnancy. (HRG Publication #1507)
Now, the same agency seems to have thrown caution to the wind and appears willing to endanger unborn babies by pretending that medical conditions such as morning sickness and edema of pregnancy are not diseases, thereby allowing the marketing of dietary supplements/herbals that have not been tested for safety.

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