Does TEZEPELUMAB-EKKO Cause Device leakage? 104 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Device leakage have been filed in association with TEZEPELUMAB-EKKO. This represents 2.4% of all adverse event reports for TEZEPELUMAB-EKKO.
104
Reports of Device leakage with TEZEPELUMAB-EKKO
2.4%
of all TEZEPELUMAB-EKKO reports
0
Deaths
7
Hospitalizations
How Dangerous Is Device leakage From TEZEPELUMAB-EKKO?
Of the 104 reports, 7 (6.7%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEZEPELUMAB-EKKO. However, 104 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which TEZEPELUMAB-EKKO Alternatives Have Lower Device leakage Risk?
TEZEPELUMAB-EKKO vs THALIDOMIDE
TEZEPELUMAB-EKKO vs THALOMID
TEZEPELUMAB-EKKO vs THEOPHYLLINE
TEZEPELUMAB-EKKO vs THEOPHYLLINE ANHYDROUS
TEZEPELUMAB-EKKO vs THIAMINE