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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SOMATOSTATIN Cause Condition aggravated? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with SOMATOSTATIN. This represents 11.2% of all adverse event reports for SOMATOSTATIN.

11
Reports of Condition aggravated with SOMATOSTATIN
11.2%
of all SOMATOSTATIN reports
5
Deaths
5
Hospitalizations

How Dangerous Is Condition aggravated From SOMATOSTATIN?

Of the 11 reports, 5 (45.5%) resulted in death, 5 (45.5%) required hospitalization, and 4 (36.4%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOMATOSTATIN. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does SOMATOSTATIN Cause?

Drug ineffective (12) Malignant neoplasm progression (12) Off label use (11) Gastrointestinal haemorrhage (10) Gastric varices (9) Portal hypertension (9) Hypersensitivity (8) Product use in unapproved indication (8) Anxiety (7) Cholelithiasis (7)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Related Pages

SOMATOSTATIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated SOMATOSTATIN Demographics