Does UNSPECIFIED INGREDIENT Cause Fibrin d dimer increased? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Fibrin d dimer increased have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
8
Reports of Fibrin d dimer increased with UNSPECIFIED INGREDIENT
0.0%
of all UNSPECIFIED INGREDIENT reports
1
Deaths
7
Hospitalizations
How Dangerous Is Fibrin d dimer increased From UNSPECIFIED INGREDIENT?
Of the 8 reports, 1 (12.5%) resulted in death, 7 (87.5%) required hospitalization.
Is Fibrin d dimer increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 8 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 Fibrin d dimer increased?
ADALIMUMAB (97)
RIVAROXABAN (91)
PREDNISONE (69)
RITUXIMAB (63)
APIXABAN (59)
ASPIRIN (54)
ACETAMINOPHEN (53)
LENALIDOMIDE (53)
METHOTREXATE (52)
BAMLANIVIMAB (49)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Fibrin d dimer increased Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN