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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 Product dose omission in error? 46 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Product dose omission in error have been filed in association with OMALIZUMAB (Omalizumab-igec). This represents 0.1% of all adverse event reports for OMALIZUMAB.

46
Reports of Product dose omission in error with OMALIZUMAB
0.1%
of all OMALIZUMAB reports
0
Deaths
10
Hospitalizations

How Dangerous Is Product dose omission in error From OMALIZUMAB?

Of the 46 reports, 10 (21.7%) required hospitalization.

Is Product dose omission in error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OMALIZUMAB. However, 46 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 Product dose omission in error?

DUPILUMAB (7,586) TOFACITINIB (2,461) LENALIDOMIDE (618) PALBOCICLIB (592) DIROXIMEL (481) ABALOPARATIDE (457) NIRAPARIB (428) RUXOLITINIB (425) TERIFLUNOMIDE (371) DIMETHYL (308)

Which OMALIZUMAB Alternatives Have Lower Product dose omission in error 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 Product dose omission in error Reports All Drugs Causing Product dose omission in error OMALIZUMAB Demographics