Does SULFAMETHOXAZOLE Cause Incorrect product administration duration? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Incorrect product administration duration have been filed in association with SULFAMETHOXAZOLE (Sulfamethoxazole and Trimethoprim DS). This represents 0.3% of all adverse event reports for SULFAMETHOXAZOLE.
13
Reports of Incorrect product administration duration with SULFAMETHOXAZOLE
0.3%
of all SULFAMETHOXAZOLE reports
11
Deaths
12
Hospitalizations
How Dangerous Is Incorrect product administration duration From SULFAMETHOXAZOLE?
Of the 13 reports, 11 (84.6%) resulted in death, 12 (92.3%) required hospitalization, and 11 (84.6%) 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 SULFAMETHOXAZOLE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does SULFAMETHOXAZOLE Cause?
Rash (2,137)
Fatigue (2,096)
Pyrexia (2,046)
Swelling (2,024)
Infection (2,018)
Joint swelling (2,017)
Hypersensitivity (2,000)
Dyspnoea (1,984)
Folliculitis (1,975)
Impaired healing (1,974)
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 SULFAMETHOXAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
SULFAMETHOXAZOLE vs SULFAMETHOXAZOLE\TRIMETHOPRIM
SULFAMETHOXAZOLE vs SULFANILAMIDE
SULFAMETHOXAZOLE vs SULFASALAZINE
SULFAMETHOXAZOLE vs SULFATHIAZOLE
SULFAMETHOXAZOLE vs SULFISOMIDINE