Does MELOXICAM Cause Product dose omission in error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product dose omission in error have been filed in association with MELOXICAM (Meloxicam). This represents 0.1% of all adverse event reports for MELOXICAM.
10
Reports of Product dose omission in error with MELOXICAM
0.1%
of all MELOXICAM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From MELOXICAM?
Of the 10 reports, 1 (10.0%) 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 MELOXICAM. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does MELOXICAM Cause?
Drug ineffective (1,815)
Arthralgia (819)
Drug hypersensitivity (776)
Pain (709)
Pain in extremity (603)
Joint swelling (566)
Peripheral swelling (557)
Dizziness (542)
Fatigue (532)
Nausea (527)
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 MELOXICAM Alternatives Have Lower Product dose omission in error Risk?
MELOXICAM vs MELPERONE
MELOXICAM vs MELPHALAN
MELOXICAM vs MEMANTINE
MELOXICAM vs MENINGOCOCCAL GROUP B VACCINE
MELOXICAM vs MENINGOCOCCAL POLYSACCHARIDE VACCINE A\NEISSERIA MENINGITIDIS GROUP A CAPSULAR POLYSACCHARIDE ANTIGEN