Does TEZEPELUMAB-EKKO Cause Product administration error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration error have been filed in association with TEZEPELUMAB-EKKO. This represents 0.2% of all adverse event reports for TEZEPELUMAB-EKKO.
8
Reports of Product administration error with TEZEPELUMAB-EKKO
0.2%
of all TEZEPELUMAB-EKKO reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From TEZEPELUMAB-EKKO?
Of the 8 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEZEPELUMAB-EKKO. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does TEZEPELUMAB-EKKO Cause?
Asthma (630)
Dyspnoea (382)
Arthralgia (381)
Drug ineffective (358)
Pneumonia (192)
Back pain (184)
Cough (182)
Rash (177)
Pain (148)
Product dose omission issue (146)
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 TEZEPELUMAB-EKKO Alternatives Have Lower Product administration error Risk?
TEZEPELUMAB-EKKO vs THALIDOMIDE
TEZEPELUMAB-EKKO vs THALOMID
TEZEPELUMAB-EKKO vs THEOPHYLLINE
TEZEPELUMAB-EKKO vs THEOPHYLLINE ANHYDROUS
TEZEPELUMAB-EKKO vs THIAMINE