Does UNSPECIFIED INGREDIENT Cause Haemoglobin decreased? 127 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 127 reports of Haemoglobin decreased have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.5% of all adverse event reports for UNSPECIFIED INGREDIENT.
127
Reports of Haemoglobin decreased with UNSPECIFIED INGREDIENT
0.5%
of all UNSPECIFIED INGREDIENT reports
21
Deaths
92
Hospitalizations
How Dangerous Is Haemoglobin decreased From UNSPECIFIED INGREDIENT?
Of the 127 reports, 21 (16.5%) resulted in death, 92 (72.4%) required hospitalization, and 13 (10.2%) 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 UNSPECIFIED INGREDIENT. However, 127 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
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 UNSPECIFIED INGREDIENT Alternatives Have Lower Haemoglobin decreased Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN