Does DYDROGESTERONE Cause Product use in unapproved indication? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product use in unapproved indication have been filed in association with DYDROGESTERONE. This represents 4.4% of all adverse event reports for DYDROGESTERONE.
15
Reports of Product use in unapproved indication with DYDROGESTERONE
4.4%
of all DYDROGESTERONE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product use in unapproved indication From DYDROGESTERONE?
Of the 15 reports, 8 (53.3%) required hospitalization.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DYDROGESTERONE. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does DYDROGESTERONE Cause?
Maternal exposure during pregnancy (117)
Abortion spontaneous (93)
Ovarian hyperstimulation syndrome (34)
Foetal exposure during pregnancy (27)
Exposure during pregnancy (20)
Off label use (18)
Meningioma (17)
Premature baby (16)
Toxicity to various agents (11)
Vaginal haemorrhage (11)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which DYDROGESTERONE Alternatives Have Lower Product use in unapproved indication Risk?
DYDROGESTERONE vs EBASTINE
DYDROGESTERONE vs ECALLANTIDE
DYDROGESTERONE vs ECONAZOLE
DYDROGESTERONE vs ECULIZUMAB
DYDROGESTERONE vs EDARAVONE