The prescriber
Get the full name and the state permission for your visit.
For a doctor, start with the state medical board. For another kind of prescriber, ask where to check the licence.
Reach your state medical boardCare questions without clinic listings
BEFORE YOU COMMIT
Start with the exact product and the names of the person who can prescribe it and the pharmacy. Ask for answers you can check.
KNOW WHAT IS BEING OFFERED
A pharmacy or doctor makes a medicine for a patient’s particular needs through a process called compounding.
A generic medicine is an approved version of the branded drug.
As of the September 26, 2026 check, the Food and Drug Administration (FDA), the U.S. drug agency, had not approved compounded medicines.
Before sale, the agency had not reviewed whether these medicines were safe, made well or worked as intended.
An FDA-approved generic form of semaglutide was not available in the United States at the September 26, 2026 check.
THE SHORTAGE QUESTION
FDA said the national shortage of semaglutide shots was over on February 21, 2025.
It gave pharmacies extra time before it planned to act over copying rules tied to that shortage.
That extra time for making pharmacy-prepared versions has ended; it did not excuse unsafe medicine or other rule breaking.
The national shortage list did not include semaglutide injections when checked September 26, 2026.
Under the rules checked September 26, 2026, pharmacies face limits on making close copies of medicines already on the market.
A health professional allowed to order medicine is known as a prescriber.
For a named patient, the prescriber can record why changing the medicine would make an important difference for that person compared with the ready-made drug.
For example, a medicine made to order can meet someone’s needs when they are allergic to a dye used in the ready-made drug.
A price saving by itself cannot qualify for this exception.
FDA’s example says adding a vitamin to a semaglutide shot at a similar strength can still leave it a copy of the ready-made drug.
Strength means how much active medicine is in the shot. Ask what is changed in your proposed medicine, why that change matters for your health, and which rules permit it.
READ THE LABEL WITH THE PRESCRIBER
The semaglutide (Wegovy) injection label lists feeling sick, vomiting, diarrhea and constipation as common effects.
It warns that severe vomiting or diarrhea can make you lose enough body water to harm your kidneys.
It also warns about gallbladder trouble, such as stones in that body part, called gallstones.
The label links severe, lasting belly pain, which may spread to the back, with painful swelling of a body part called the pancreas.
This can be a serious problem; the label tells prescribers to stop the medicine if they suspect it.
Ask before treatment whom to call promptly if this pain appears, and when to get emergency help. Ask what to do if you cannot reach that person.
The label’s warning about a body part called the thyroid lists neck lumps among the signs to discuss with the prescriber.
Semaglutide labels give their most prominent warning, a boxed warning, for these tumors seen in rats and mice; tumors are growths.
Whether semaglutide causes those tumors in people remains unknown, according to the labels.
Ask which parts of your history affect the choice and how new symptoms would be handled.
MAKE THE CHECKS CONCRETE
Get the full name and the state permission for your visit.
For a doctor, start with the state medical board. For another kind of prescriber, ask where to check the licence.
Reach your state medical boardAsk which pharmacy dispenses the medicine, then use the state licence search.
Open FDA’s state pharmacy searchA pharmacy licence record confirms a licence, not whether every prescription is being filled appropriately.
Under U.S. rules checked September 26, 2026, the law barred giving out a prescription medicine if there was no valid prescription.
Under rules checked September 26, 2026, “FDA registered” meant recorded with the agency; it did not show FDA had approved the business or its medicine.
Registration also does not establish that the medicine can lawfully be sold.
Emergency care is needed for a severe allergic reaction.
MedlinePlus lists swelling of the tongue or face and difficulty breathing among the symptoms, and calls for emergency help if symptoms are severe.
THE SOURCE NOTES
Read the original guidance, records and research.
The legal-status notes reflect the September 26, 2026 check.
The label information was checked September 26, 2026.
Use the state board for the licence record.