Does TEPROTUMUMAB-TRBW Cause Product administration error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with TEPROTUMUMAB-TRBW. This represents 0.1% of all adverse event reports for TEPROTUMUMAB-TRBW.
6
Reports of Product administration error with TEPROTUMUMAB-TRBW
0.1%
of all TEPROTUMUMAB-TRBW reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From TEPROTUMUMAB-TRBW?
Of the 6 reports, 1 (16.7%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEPROTUMUMAB-TRBW. However, 6 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which TEPROTUMUMAB-TRBW Alternatives Have Lower Product administration error Risk?
TEPROTUMUMAB-TRBW vs TERAZOSIN
TEPROTUMUMAB-TRBW vs TERAZOSIN\TERAZOSIN
TEPROTUMUMAB-TRBW vs TERBINAFINE
TEPROTUMUMAB-TRBW vs TERBINAFINE\TERBINAFINE
TEPROTUMUMAB-TRBW vs TERBUTALINE