Does TEPROTUMUMAB-TRBW Cause Condition aggravated? 188 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 188 reports of Condition aggravated have been filed in association with TEPROTUMUMAB-TRBW. This represents 3.8% of all adverse event reports for TEPROTUMUMAB-TRBW.
188
Reports of Condition aggravated with TEPROTUMUMAB-TRBW
3.8%
of all TEPROTUMUMAB-TRBW reports
0
Deaths
20
Hospitalizations
How Dangerous Is Condition aggravated From TEPROTUMUMAB-TRBW?
Of the 188 reports, 20 (10.6%) required hospitalization, and 1 (0.5%) 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 TEPROTUMUMAB-TRBW. However, 188 reports have been filed with the FAERS database.
What Other Side Effects Does TEPROTUMUMAB-TRBW Cause?
Muscle spasms (998)
Fatigue (704)
Tinnitus (524)
Headache (443)
Hypoacusis (430)
Diarrhoea (408)
Nausea (407)
Blood glucose increased (401)
Alopecia (390)
Pain (344)
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 TEPROTUMUMAB-TRBW Alternatives Have Lower Condition aggravated Risk?
TEPROTUMUMAB-TRBW vs TERAZOSIN
TEPROTUMUMAB-TRBW vs TERAZOSIN\TERAZOSIN
TEPROTUMUMAB-TRBW vs TERBINAFINE
TEPROTUMUMAB-TRBW vs TERBINAFINE\TERBINAFINE
TEPROTUMUMAB-TRBW vs TERBUTALINE