Does MORPHINE Cause Product dose omission issue? 255 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 255 reports of Product dose omission issue have been filed in association with MORPHINE (Morphine Sulfate). This represents 0.2% of all adverse event reports for MORPHINE.
255
Reports of Product dose omission issue with MORPHINE
0.2%
of all MORPHINE reports
21
Deaths
168
Hospitalizations
How Dangerous Is Product dose omission issue From MORPHINE?
Of the 255 reports, 21 (8.2%) resulted in death, 168 (65.9%) required hospitalization, and 17 (6.7%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MORPHINE. However, 255 reports have been filed with the FAERS database.
What Other Side Effects Does MORPHINE Cause?
Drug dependence (40,036)
Overdose (26,942)
Pain (22,787)
Death (17,960)
Emotional distress (17,954)
Toxicity to various agents (15,337)
Drug withdrawal syndrome (14,954)
Drug hypersensitivity (11,095)
Drug abuse (6,636)
Dependence (5,656)
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 MORPHINE Alternatives Have Lower Product dose omission issue Risk?
MORPHINE vs MORPHINE\NALTREXONE
MORPHINE vs MOSAPRIDE
MORPHINE vs MOSUNETUZUMAB
MORPHINE vs MOSUNETUZUMAB-AXGB
MORPHINE vs MOXIFLOXACIN