Does TRAMADOL Cause Product dose omission issue? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Product dose omission issue have been filed in association with TRAMADOL (ConZip). This represents 0.1% of all adverse event reports for TRAMADOL.
71
Reports of Product dose omission issue with TRAMADOL
0.1%
of all TRAMADOL reports
5
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission issue From TRAMADOL?
Of the 71 reports, 5 (7.0%) resulted in death, 17 (23.9%) required hospitalization, and 2 (2.8%) 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 TRAMADOL. However, 71 reports have been filed with the FAERS database.
What Other Side Effects Does TRAMADOL Cause?
Drug dependence (21,018)
Overdose (12,705)
Dependence (8,530)
Pain (7,758)
Toxicity to various agents (5,252)
Emotional distress (4,901)
Drug abuse (4,553)
Vomiting (4,396)
Drug hypersensitivity (4,052)
Death (4,012)
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 TRAMADOL Alternatives Have Lower Product dose omission issue Risk?
TRAMADOL vs TRAMADOL\TRAMADOL
TRAMADOL vs TRAMETINIB
TRAMADOL vs TRAMETINIB DIMETHYL SULFOXIDE
TRAMADOL vs TRANDOLAPRIL
TRAMADOL vs TRANDOLAPRIL\VERAPAMIL