Does DICLOFENAC\MISOPROSTOL Cause Condition aggravated? 174 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 174 reports of Condition aggravated have been filed in association with DICLOFENAC\MISOPROSTOL. This represents 11.1% of all adverse event reports for DICLOFENAC\MISOPROSTOL.
174
Reports of Condition aggravated with DICLOFENAC\MISOPROSTOL
11.1%
of all DICLOFENAC\MISOPROSTOL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Condition aggravated From DICLOFENAC\MISOPROSTOL?
Of the 174 reports, 3 (1.7%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC\MISOPROSTOL. However, 174 reports have been filed with the FAERS database.
What Other Side Effects Does DICLOFENAC\MISOPROSTOL Cause?
Drug ineffective (478)
Drug hypersensitivity (384)
Rheumatoid arthritis (271)
Pain (220)
Drug intolerance (194)
Infection (189)
Nausea (180)
Arthralgia (147)
International normalised ratio fluctuation (144)
Malaise (139)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DICLOFENAC\MISOPROSTOL Alternatives Have Lower Condition aggravated Risk?
DICLOFENAC\MISOPROSTOL vs DICLOXACILLIN
DICLOFENAC\MISOPROSTOL vs DICYCLOMINE
DICLOFENAC\MISOPROSTOL vs DIDANOSINE
DICLOFENAC\MISOPROSTOL vs DIENOGEST
DICLOFENAC\MISOPROSTOL vs DIENOGEST\ESTRADIOL