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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TEZEPELUMAB-EKKO Cause Device malfunction? 53 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Device malfunction have been filed in association with TEZEPELUMAB-EKKO. This represents 1.2% of all adverse event reports for TEZEPELUMAB-EKKO.

53
Reports of Device malfunction with TEZEPELUMAB-EKKO
1.2%
of all TEZEPELUMAB-EKKO reports
0
Deaths
3
Hospitalizations

How Dangerous Is Device malfunction From TEZEPELUMAB-EKKO?

Of the 53 reports, 3 (5.7%) required hospitalization, and 1 (1.9%) were considered life-threatening.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TEZEPELUMAB-EKKO. However, 53 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 malfunction?

PEGFILGRASTIM (6,818) EXENATIDE (3,273) BUDESONIDE\FORMOTEROL (2,771) ABATACEPT (2,459) SOMATROPIN (2,311) GOLIMUMAB (2,293) SECUKINUMAB (2,259) ALBUTEROL (2,257) GUSELKUMAB (1,410) MOMETASONE FUROATE (1,332)

Which TEZEPELUMAB-EKKO Alternatives Have Lower Device malfunction Risk?

TEZEPELUMAB-EKKO vs THALIDOMIDE TEZEPELUMAB-EKKO vs THALOMID TEZEPELUMAB-EKKO vs THEOPHYLLINE TEZEPELUMAB-EKKO vs THEOPHYLLINE ANHYDROUS TEZEPELUMAB-EKKO vs THIAMINE

Related Pages

TEZEPELUMAB-EKKO Full Profile All Device malfunction Reports All Drugs Causing Device malfunction TEZEPELUMAB-EKKO Demographics