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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 PROCHLORPERAZINE Cause Haemoglobin decreased? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Haemoglobin decreased have been filed in association with PROCHLORPERAZINE (PROCHLORPERAZINE MALEATE). This represents 1.0% of all adverse event reports for PROCHLORPERAZINE.

22
Reports of Haemoglobin decreased with PROCHLORPERAZINE
1.0%
of all PROCHLORPERAZINE reports
2
Deaths
12
Hospitalizations

How Dangerous Is Haemoglobin decreased From PROCHLORPERAZINE?

Of the 22 reports, 2 (9.1%) resulted in death, 12 (54.5%) required hospitalization, and 2 (9.1%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROCHLORPERAZINE. However, 22 reports have been filed with the FAERS database.

What Other Side Effects Does PROCHLORPERAZINE Cause?

Nausea (523) Drug hypersensitivity (452) Vomiting (317) Fatigue (308) Headache (255) Drug ineffective (237) Asthenia (218) Cough (215) Rheumatoid arthritis (215) Pain (209)

What Other Drugs Cause Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which PROCHLORPERAZINE Alternatives Have Lower Haemoglobin decreased Risk?

PROCHLORPERAZINE vs PROCHLORPERAZINE EDISYLATE PROCHLORPERAZINE vs PROCRIT PROCHLORPERAZINE vs PROCYCLIDINE PROCHLORPERAZINE vs PROGESTERONE PROCHLORPERAZINE vs PROGRAF

Related Pages

PROCHLORPERAZINE Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased PROCHLORPERAZINE Demographics