Does TEZEPELUMAB-EKKO Cause Device issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Device issue have been filed in association with TEZEPELUMAB-EKKO. This represents 0.6% of all adverse event reports for TEZEPELUMAB-EKKO.
28
Reports of Device issue with TEZEPELUMAB-EKKO
0.6%
of all TEZEPELUMAB-EKKO reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device issue From TEZEPELUMAB-EKKO?
Of the 28 reports, 3 (10.7%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEZEPELUMAB-EKKO. However, 28 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which TEZEPELUMAB-EKKO Alternatives Have Lower Device issue Risk?
TEZEPELUMAB-EKKO vs THALIDOMIDE
TEZEPELUMAB-EKKO vs THALOMID
TEZEPELUMAB-EKKO vs THEOPHYLLINE
TEZEPELUMAB-EKKO vs THEOPHYLLINE ANHYDROUS
TEZEPELUMAB-EKKO vs THIAMINE