Does BACLOFEN Cause Product dose omission issue? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Product dose omission issue have been filed in association with BACLOFEN (BACLOFEN). This represents 0.3% of all adverse event reports for BACLOFEN.
65
Reports of Product dose omission issue with BACLOFEN
0.3%
of all BACLOFEN reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission issue From BACLOFEN?
Of the 65 reports, 24 (36.9%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BACLOFEN. However, 65 reports have been filed with the FAERS database.
What Other Side Effects Does BACLOFEN Cause?
Muscle spasticity (2,893)
Drug withdrawal syndrome (2,284)
Pain (2,048)
Toxicity to various agents (1,868)
Overdose (1,554)
Off label use (1,454)
Drug ineffective (1,445)
Somnolence (1,433)
Muscle spasms (1,279)
Coma (1,133)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which BACLOFEN Alternatives Have Lower Product dose omission issue Risk?
BACLOFEN vs BACLOFEN INTRATHECAL
BACLOFEN vs BACTRIM
BACLOFEN vs BALOXAVIR MARBOXIL
BACLOFEN vs BALSALAZIDE
BACLOFEN vs BAMLANIVIMAB