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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 GALCANEZUMAB Cause Product dose omission? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission have been filed in association with GALCANEZUMAB (EMGALITY). This represents 3.7% of all adverse event reports for GALCANEZUMAB.

14
Reports of Product dose omission with GALCANEZUMAB
3.7%
of all GALCANEZUMAB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product dose omission From GALCANEZUMAB?

Of the 14 reports.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GALCANEZUMAB. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does GALCANEZUMAB Cause?

Injection site pain (66) Drug ineffective (39) Underdose (33) Headache (31) Migraine (30) Off label use (22) Constipation (19) Hypersensitivity (11) Injection site haemorrhage (11) Dizziness (10)

What Other Drugs Cause Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which GALCANEZUMAB Alternatives Have Lower Product dose omission Risk?

GALCANEZUMAB vs GALCANEZUMAB-GNLM GALCANEZUMAB vs GALLIUM GA-OZETOTIDE GALCANEZUMAB vs GALSULFASE GALCANEZUMAB vs GAMMAGARD LIQUID GALCANEZUMAB vs GANAXOLONE

Related Pages

GALCANEZUMAB Full Profile All Product dose omission Reports All Drugs Causing Product dose omission GALCANEZUMAB Demographics