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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 Device failure? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device failure have been filed in association with PROGESTERONE (Progesterone). This represents 0.1% of all adverse event reports for PROGESTERONE.

5
Reports of Device failure with PROGESTERONE
0.1%
of all PROGESTERONE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device failure From PROGESTERONE?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 5 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 Device failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which PROGESTERONE Alternatives Have Lower Device failure Risk?

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

Related Pages

PROGESTERONE Full Profile All Device failure Reports All Drugs Causing Device failure PROGESTERONE Demographics