Does ETANERCEPT Cause Maternal exposure timing unspecified? 261 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 261 reports of Maternal exposure timing unspecified have been filed in association with ETANERCEPT (ENBREL). This represents 0.1% of all adverse event reports for ETANERCEPT.
261
Reports of Maternal exposure timing unspecified with ETANERCEPT
0.1%
of all ETANERCEPT reports
149
Deaths
173
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ETANERCEPT?
Of the 261 reports, 149 (57.1%) resulted in death, 173 (66.3%) required hospitalization, and 164 (62.8%) 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 ETANERCEPT. However, 261 reports have been filed with the FAERS database.
What Other Side Effects Does ETANERCEPT Cause?
Drug ineffective (60,367)
Rheumatoid arthritis (33,166)
Pain (31,961)
Arthralgia (27,429)
Injection site pain (24,717)
Off label use (20,178)
Fatigue (19,907)
Joint swelling (18,462)
Injection site erythema (17,736)
Condition aggravated (15,897)
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 ETANERCEPT Alternatives Have Lower Maternal exposure timing unspecified Risk?
ETANERCEPT vs ETANERCEPT-SZZS
ETANERCEPT vs ETELCALCETIDE
ETANERCEPT vs ETEPLIRSEN
ETANERCEPT vs ETESEVIMAB
ETANERCEPT vs ETHACRYNIC ACID