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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 DROMOSTANOLONE Cause Product use issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use issue have been filed in association with DROMOSTANOLONE. This represents 8.5% of all adverse event reports for DROMOSTANOLONE.

6
Reports of Product use issue with DROMOSTANOLONE
8.5%
of all DROMOSTANOLONE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product use issue From DROMOSTANOLONE?

Of the 6 reports, 6 (100.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DROMOSTANOLONE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does DROMOSTANOLONE Cause?

Drug abuse (31) Intentional product misuse (16) Secondary hypogonadism (10) Autoimmune thyroiditis (9) Diabetes mellitus (9) Multiple organ dysfunction syndrome (9) Hepatic neoplasm (8) Poisoning (8) Haematocrit increased (7) Intra-abdominal haemorrhage (7)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

DROMOSTANOLONE Full Profile All Product use issue Reports All Drugs Causing Product use issue DROMOSTANOLONE Demographics