Does GALCANEZUMAB-GNLM Cause Wrong technique in product usage process? 138 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 138 reports of Wrong technique in product usage process have been filed in association with GALCANEZUMAB-GNLM. This represents 0.5% of all adverse event reports for GALCANEZUMAB-GNLM.
138
Reports of Wrong technique in product usage process with GALCANEZUMAB-GNLM
0.5%
of all GALCANEZUMAB-GNLM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From GALCANEZUMAB-GNLM?
Of the 138 reports, 2 (1.4%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GALCANEZUMAB-GNLM. However, 138 reports have been filed with the FAERS database.
What Other Side Effects Does GALCANEZUMAB-GNLM Cause?
Injection site pain (6,622)
Underdose (2,909)
Migraine (2,612)
Headache (2,104)
Drug ineffective (1,610)
Product dose omission issue (1,591)
Injection site haemorrhage (1,415)
Accidental underdose (1,064)
Injection site erythema (1,052)
Injection site pruritus (774)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which GALCANEZUMAB-GNLM Alternatives Have Lower Wrong technique in product usage process Risk?
GALCANEZUMAB-GNLM vs GALLIUM GA-OZETOTIDE
GALCANEZUMAB-GNLM vs GALSULFASE
GALCANEZUMAB-GNLM vs GAMMAGARD LIQUID
GALCANEZUMAB-GNLM vs GANAXOLONE
GALCANEZUMAB-GNLM vs GANCICLOVIR