Does MISOPROSTOL Cause Maternal exposure timing unspecified? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Maternal exposure timing unspecified have been filed in association with MISOPROSTOL (Misoprostol). This represents 0.6% of all adverse event reports for MISOPROSTOL.
21
Reports of Maternal exposure timing unspecified with MISOPROSTOL
0.6%
of all MISOPROSTOL reports
7
Deaths
8
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From MISOPROSTOL?
Of the 21 reports, 7 (33.3%) resulted in death, 8 (38.1%) required hospitalization, and 3 (14.3%) 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 MISOPROSTOL. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does MISOPROSTOL Cause?
Off label use (632)
Haemorrhage (588)
Abortion incomplete (535)
Product use in unapproved indication (296)
Maternal exposure during pregnancy (261)
Pain (231)
Foetal exposure during pregnancy (221)
Foetal exposure during delivery (204)
Drug ineffective (190)
Anaemia (185)
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 MISOPROSTOL Alternatives Have Lower Maternal exposure timing unspecified Risk?
MISOPROSTOL vs MITAPIVAT
MISOPROSTOL vs MITOMYCIN
MISOPROSTOL vs MITOTANE
MISOPROSTOL vs MITOXANTRONE
MISOPROSTOL vs MITRAGYNINE\HERBALS