Does PROGESTERONE Cause Maternal exposure timing unspecified? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Maternal exposure timing unspecified have been filed in association with PROGESTERONE (Progesterone). This represents 0.2% of all adverse event reports for PROGESTERONE.
9
Reports of Maternal exposure timing unspecified with PROGESTERONE
0.2%
of all PROGESTERONE reports
2
Deaths
4
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From PROGESTERONE?
Of the 9 reports, 2 (22.2%) resulted in death, 4 (44.4%) required hospitalization, and 2 (22.2%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 9 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which PROGESTERONE Alternatives Have Lower Maternal exposure timing unspecified Risk?
PROGESTERONE vs PROGRAF
PROGESTERONE vs PROHANCE
PROGESTERONE vs PROLIA
PROGESTERONE vs PROMACTA
PROGESTERONE vs PROMAZINE