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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 BUDESONIDE Cause Fibrin d dimer increased? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Fibrin d dimer increased have been filed in association with BUDESONIDE (BREYNA). This represents 0.0% of all adverse event reports for BUDESONIDE.

7
Reports of Fibrin d dimer increased with BUDESONIDE
0.0%
of all BUDESONIDE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Fibrin d dimer increased From BUDESONIDE?

Of the 7 reports, 4 (57.1%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Fibrin d dimer increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does BUDESONIDE Cause?

Asthma (4,544) Dyspnoea (4,441) Drug ineffective (4,384) Off label use (3,033) Wheezing (2,590) Cough (2,269) Therapeutic product effect incomplete (2,191) Loss of personal independence in daily activities (1,890) Condition aggravated (1,548) Fatigue (1,508)

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 BUDESONIDE Alternatives Have Lower Fibrin d dimer increased Risk?

BUDESONIDE vs BUDESONIDE\FORMOTEROL BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM BUDESONIDE vs BUMETANIDE BUDESONIDE vs BUPIVACAINE

Related Pages

BUDESONIDE Full Profile All Fibrin d dimer increased Reports All Drugs Causing Fibrin d dimer increased BUDESONIDE Demographics