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Antibiotics & Antidepressants on Top of the FDA Watch List

Antibiotics & Antidepressants on Top of the FDA Watch List

What Happens When The FDA Is Addicted To The Drug Industry?

What Happens When The FDA Is Addicted To The Drug Industry?

Why Isn’t the FDA Tougher on Tainted Supplements?

Why Isn’t the FDA Tougher on Tainted Supplements?

Open Letter to the FDA: You’re Protecting the Wrong People

Su Calls on the FDA to Release the Names of Drugs Approved Using Fraudulent Data

Open Letter to the FDA: You’re Protecting the Wrong People

Suzanne B. Robotti

'Pink Viagra'? Why We Shouldn't Rush to 'Fix' Women's Bodies

‘Pink Viagra’? Why We Shouldn’t Rush to ‘Fix’ Women’s Bodies

Medshadow Staff

FDA Finds Eye Injections Caused Vision Impairment

FDA Finds Eye Injections Caused Vision Impairment

Prescription Drug Advertising May Soon Come to Twitter

Prescription Drug Advertising May Soon Come to Twitter

fda safety update, pills

MedShadow Articles

FDA Side Effects Update: Jylamvo, Limbitrol, Liptruzet, and More

FDA Advisory Committee and FDA Drug Approval

Advice for FDA Drug Approvals

Suzanne B. Robotti

Do Clinical Trials Discriminate Against Women?

FDA FDA Watch Issues Related to Healthcare Tests and Testing Treatments

Do Clinical Trials Discriminate Against Women?

Family Dollar Recall

Family Dollar Products Recalled Due to Contamination

What to Know About the Right to Try Law in 2024

What to Know About the Right to Try Law in 2024

MedShadow Articles

Choices For The Terminally Ill: FDA’S Expanded Access Program Or Right To Try Act?

Jessica DiGiacinto

Faster FDA Approvals

Issues Related to Healthcare

Faster FDA Approvals = More Drug Safety Problems

Natural Weight Loss Herb (Bethel) Contains Unnatural Drug (Sibutramine)

Drug Interactions/Side Effects

Bethel Herb: Natural, Yet Contains Unnatural Sibutramine Drug

Suzanne B. Robotti

Heart Failure Drug Rejected, Rejected Again, Then Approved, What’s Up?

MedShadow Articles

Heart Failure Drug Rejected, Rejected Again, Then Approved, What’s Up?

Why The FDA Withdrew Emergency Use Status For Hydroxychloroquine

Why The FDA Withdrew Emergency Use Status For Hydroxychloroquine

FDA

Quick Hits: FDA Decisions and FDA Approvals

The FDA Calls For Opana's Removal From The Market

The FDA Calls For Opana’s Removal From The Market

Did Hype Drive the FDA Decision on Addyi (Flibanserin)?

Did Hype Drive the FDA Decision on Addyi (Flibanserin)?

Required Postmarketing Studies For New Drugs

Required Postmarketing Studies For New Drugs

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