Does UNSPECIFIED INGREDIENT Cause Abdominal distension? 249 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 249 reports of Abdominal distension have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
249
Reports of Abdominal distension with UNSPECIFIED INGREDIENT
1.0%
of all UNSPECIFIED INGREDIENT reports
131
Deaths
143
Hospitalizations
How Dangerous Is Abdominal distension From UNSPECIFIED INGREDIENT?
Of the 249 reports, 131 (52.6%) resulted in death, 143 (57.4%) required hospitalization, and 86 (34.5%) were considered life-threatening.
Is Abdominal distension Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 249 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause Abdominal distension?
ADALIMUMAB (3,728)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,238)
LEVONORGESTREL (1,700)
METHOTREXATE (1,471)
TREPROSTINIL (1,437)
PREDNISONE (1,429)
SEMAGLUTIDE (1,424)
VEDOLIZUMAB (1,411)
INFLIXIMAB (1,328)
POLYETHYLENE GLYCOL 3350 (1,158)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Abdominal distension Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN