FDA Drug Shortages: What’s Causing Them and How It Affects Your Medications

When the FDA drug shortages, officially reported gaps in the supply of essential medications approved by the U.S. Food and Drug Administration. Also known as medication shortages, these aren’t just inconveniences—they can delay life-saving treatments, force risky switches, and push patients toward more expensive or less effective options. This isn’t rare. In 2023 alone, over 300 drugs were listed as in short supply by the FDA, from antibiotics and chemotherapy agents to common generics like metformin and levothyroxine. These aren’t niche drugs—they’re the ones millions rely on every day.

FDA drug shortages don’t happen because no one makes the drug. They happen because of broken links in the drug supply chain, the complex network of manufacturers, raw material suppliers, distributors, and regulators that keeps medications moving from factory to pharmacy. One factory with poor quality control can shut down production for months. A single raw ingredient from overseas can get stuck in customs. If only one company makes a cheap generic—and they can’t scale up or face a recall—there’s no backup. That’s what happened with injectable epinephrine in 2022: one plant failure left hospitals scrambling. Meanwhile, generic drug availability, the reliability of low-cost versions of brand-name drugs that make up over 90% of prescriptions in the U.S.. is under constant pressure. Manufacturers often skip making low-margin generics because they’re not profitable enough, even when they’re medically essential.

It’s not just about running out of pills. When a drug is in short supply, pharmacies may give you a different brand, a higher dose, or a less familiar formulation. That’s risky if you’re on multiple meds or have allergies. Some patients end up paying hundreds more just to get the same treatment. Others wait weeks, skipping doses or splitting pills—both dangerous moves. The FDA tracks these shortages, but they don’t fix them. They only warn you after the fact.

What you can do? Know your meds. Keep a list of your prescriptions with both brand and generic names. Ask your pharmacist: "Is this the only version available?" If your medication is on the FDA’s shortage list, they can often suggest alternatives or help you get it through a specialty distributor. Don’t assume your next refill will be the same. Stay ahead, ask questions, and don’t let silence from your pharmacy mean everything’s fine.

The posts below cover real situations where drug shortages hit hard—from switching pharmacies under pressure, to understanding why your generic suddenly cost 300% more, to how pharmacogenomics can help avoid dangerous substitutions. You’ll find practical guides on managing your meds when supply is unstable, how to spot when a drug change is risky, and what to say to your doctor when your usual treatment disappears.

FDA Generic Approval Changes 2023-2025: What Manufacturers and Patients Need to Know

The FDA's 2023-2025 updates to generic drug approval are reshaping how medicines are made and accessed in the U.S. Faster approvals for U.S.-made generics are reducing shortages-but at a cost.