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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 Intentional product use issue? 42 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Intentional product use issue have been filed in association with PROGESTERONE (Progesterone). This represents 0.8% of all adverse event reports for PROGESTERONE.

42
Reports of Intentional product use issue with PROGESTERONE
0.8%
of all PROGESTERONE reports
4
Deaths
7
Hospitalizations

How Dangerous Is Intentional product use issue From PROGESTERONE?

Of the 42 reports, 4 (9.5%) resulted in death, 7 (16.7%) required hospitalization, and 1 (2.4%) were considered life-threatening.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 42 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 Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which PROGESTERONE Alternatives Have Lower Intentional product use issue Risk?

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

Related Pages

PROGESTERONE Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue PROGESTERONE Demographics