Does TRAMADOL Cause Incorrect product administration duration? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Incorrect product administration duration have been filed in association with TRAMADOL (ConZip). This represents 0.1% of all adverse event reports for TRAMADOL.
98
Reports of Incorrect product administration duration with TRAMADOL
0.1%
of all TRAMADOL reports
61
Deaths
64
Hospitalizations
How Dangerous Is Incorrect product administration duration From TRAMADOL?
Of the 98 reports, 61 (62.2%) resulted in death, 64 (65.3%) required hospitalization, and 61 (62.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRAMADOL. However, 98 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TRAMADOL Alternatives Have Lower Incorrect product administration duration Risk?
TRAMADOL vs TRAMADOL\TRAMADOL
TRAMADOL vs TRAMETINIB
TRAMADOL vs TRAMETINIB DIMETHYL SULFOXIDE
TRAMADOL vs TRANDOLAPRIL
TRAMADOL vs TRANDOLAPRIL\VERAPAMIL