Does VALPROATE Cause Haemoglobin decreased? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Haemoglobin decreased have been filed in association with VALPROATE (Valproate Sodium). This represents 0.4% of all adverse event reports for VALPROATE.
59
Reports of Haemoglobin decreased with VALPROATE
0.4%
of all VALPROATE reports
4
Deaths
30
Hospitalizations
How Dangerous Is Haemoglobin decreased From VALPROATE?
Of the 59 reports, 4 (6.8%) resulted in death, 30 (50.8%) required hospitalization, and 8 (13.6%) 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 VALPROATE. However, 59 reports have been filed with the FAERS database.
What Other Side Effects Does VALPROATE Cause?
Foetal exposure during pregnancy (1,982)
Drug ineffective (1,268)
Seizure (1,083)
Epilepsy (878)
Somnolence (843)
Off label use (744)
Drug abuse (705)
Sopor (577)
Dysmorphism (552)
Drug interaction (513)
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 VALPROATE Alternatives Have Lower Haemoglobin decreased Risk?
VALPROATE vs VALPROIC ACID
VALPROATE vs VALPROMIDE
VALPROATE vs VALSARTAN
VALPROATE vs VALTREX
VALPROATE vs VAMOROLONE