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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PROGESTERONE Cause Wrong product administered? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong product administered have been filed in association with PROGESTERONE (Progesterone). This represents 0.1% of all adverse event reports for PROGESTERONE.

6
Reports of Wrong product administered with PROGESTERONE
0.1%
of all PROGESTERONE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Wrong product administered From PROGESTERONE?

Of the 6 reports, 2 (33.3%) required hospitalization, and 1 (16.7%) were considered life-threatening.

Is Wrong product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does PROGESTERONE Cause?

Off label use (736) Headache (701) Exposure during pregnancy (684) Pain (591) Hypersensitivity (579) Product use issue (542) Fatigue (535) Hyperhidrosis (534) Drug hypersensitivity (512) Hepatic enzyme increased (509)

What Other Drugs Cause Wrong product administered?

INSULIN LISPRO (337) INSULIN GLARGINE (226) RISPERIDONE (141) QUETIAPINE (137) ACETAMINOPHEN (133) INSULIN ASPART (112) CLOZAPINE (106) INSULIN HUMAN (104) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104) IBUPROFEN (102)

Which PROGESTERONE Alternatives Have Lower Wrong product administered Risk?

PROGESTERONE vs PROGRAF PROGESTERONE vs PROHANCE PROGESTERONE vs PROLIA PROGESTERONE vs PROMACTA PROGESTERONE vs PROMAZINE

Related Pages

PROGESTERONE Full Profile All Wrong product administered Reports All Drugs Causing Wrong product administered PROGESTERONE Demographics