Does BARICITINIB Cause Wrong technique in product usage process? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Wrong technique in product usage process have been filed in association with BARICITINIB (Olumiant). This represents 0.1% of all adverse event reports for BARICITINIB.
11
Reports of Wrong technique in product usage process with BARICITINIB
0.1%
of all BARICITINIB reports
1
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From BARICITINIB?
Of the 11 reports, 1 (9.1%) resulted in death, 2 (18.2%) 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 BARICITINIB. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does BARICITINIB Cause?
Drug ineffective (569)
Off label use (479)
Covid-19 (347)
Pulmonary embolism (288)
Rheumatoid arthritis (284)
Headache (216)
Herpes zoster (216)
Pneumonia (216)
Death (206)
Deep vein thrombosis (201)
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 BARICITINIB Alternatives Have Lower Wrong technique in product usage process Risk?
BARICITINIB vs BARIUM
BARICITINIB vs BARNIDIPINE
BARICITINIB vs BASILIXIMAB
BARICITINIB vs BAYER GENUINE ASPIRIN ORIGINAL STRENGTH
BARICITINIB vs BAZEDOXIFENE\ESTROGENS, CONJUGATED