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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 PROCYCLIDINE Cause Condition aggravated? 170 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Condition aggravated have been filed in association with PROCYCLIDINE. This represents 25.6% of all adverse event reports for PROCYCLIDINE.

170
Reports of Condition aggravated with PROCYCLIDINE
25.6%
of all PROCYCLIDINE reports
1
Deaths
168
Hospitalizations

How Dangerous Is Condition aggravated From PROCYCLIDINE?

Of the 170 reports, 1 (0.6%) resulted in death, 168 (98.8%) required hospitalization, and 6 (3.5%) 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 PROCYCLIDINE. However, 170 reports have been filed with the FAERS database.

What Other Side Effects Does PROCYCLIDINE Cause?

Vomiting (248) Schizophrenia (223) Pneumonia (203) Nausea (195) Cholelithiasis (192) Psychotic disorder (179) Hepatic enzyme increased (138) Blood bilirubin increased (132) Hepatotoxicity (132) Jaundice cholestatic (132)

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 PROCYCLIDINE Alternatives Have Lower Condition aggravated Risk?

PROCYCLIDINE vs PROGESTERONE PROCYCLIDINE vs PROGRAF PROCYCLIDINE vs PROHANCE PROCYCLIDINE vs PROLIA PROCYCLIDINE vs PROMACTA

Related Pages

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