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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 DROPERIDOL Cause Condition aggravated? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Condition aggravated have been filed in association with DROPERIDOL (Droperidol). This represents 2.1% of all adverse event reports for DROPERIDOL.

19
Reports of Condition aggravated with DROPERIDOL
2.1%
of all DROPERIDOL reports
1
Deaths
9
Hospitalizations

How Dangerous Is Condition aggravated From DROPERIDOL?

Of the 19 reports, 1 (5.3%) resulted in death, 9 (47.4%) required hospitalization, and 8 (42.1%) 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 DROPERIDOL. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does DROPERIDOL Cause?

Anaphylactic shock (105) Drug hypersensitivity (64) Hypotension (51) Anaphylactic reaction (48) Tachycardia (41) Acute kidney injury (37) Vomiting (34) Rash (33) Cardiac arrest (30) Drug ineffective (30)

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)

Which DROPERIDOL Alternatives Have Lower Condition aggravated Risk?

DROPERIDOL vs DROSPIRENONE DROPERIDOL vs DROSPIRENONE\ESTETROL DROPERIDOL vs DROSPIRENONE\ESTRADIOL DROPERIDOL vs DROSPIRENONE\ETHINYL ESTRADIOL DROPERIDOL vs DROSPIRENONE\ETHINYL ESTRADIOL\LEVOMEFOLATE

Related Pages

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