Does PROGESTERONE Cause Recalled product administered? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Recalled product administered have been filed in association with PROGESTERONE (Progesterone). This represents 0.3% of all adverse event reports for PROGESTERONE.
18
Reports of Recalled product administered with PROGESTERONE
0.3%
of all PROGESTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product administered From PROGESTERONE?
Of the 18 reports, 1 (5.6%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 18 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which PROGESTERONE Alternatives Have Lower Recalled product administered Risk?
PROGESTERONE vs PROGRAF
PROGESTERONE vs PROHANCE
PROGESTERONE vs PROLIA
PROGESTERONE vs PROMACTA
PROGESTERONE vs PROMAZINE