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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 OMALIZUMAB Cause Device malfunction? 179 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 179 reports of Device malfunction have been filed in association with OMALIZUMAB (Omalizumab-igec). This represents 0.3% of all adverse event reports for OMALIZUMAB.

179
Reports of Device malfunction with OMALIZUMAB
0.3%
of all OMALIZUMAB reports
2
Deaths
5
Hospitalizations

How Dangerous Is Device malfunction From OMALIZUMAB?

Of the 179 reports, 2 (1.1%) resulted in death, 5 (2.8%) required hospitalization, and 1 (0.6%) 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 OMALIZUMAB. However, 179 reports have been filed with the FAERS database.

What Other Side Effects Does OMALIZUMAB Cause?

No adverse event (9,736) Asthma (9,354) Urticaria (9,231) Off label use (9,199) Dyspnoea (8,323) Drug ineffective (6,747) Cough (5,926) Pruritus (5,224) Fatigue (5,053) Malaise (4,820)

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 OMALIZUMAB Alternatives Have Lower Device malfunction Risk?

OMALIZUMAB vs OMAVELOXOLONE OMALIZUMAB vs OMBITASVIR OMALIZUMAB vs OMBITASVIR\PARITAPREVIR\RITONAVIR OMALIZUMAB vs OMEGA-3-ACID ETHYL ESTERS OMALIZUMAB vs OMEGA-3-CARBOXYLIC ACIDS

Related Pages

OMALIZUMAB Full Profile All Device malfunction Reports All Drugs Causing Device malfunction OMALIZUMAB Demographics