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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.

FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE for Pulmonary fibrosis: Side Effects & Safety Data

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There are 40 adverse event reports in the FDA FAERS database where FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE was used for Pulmonary fibrosis.

Most Reported Side Effects for FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE

Side Effect Reports % Deaths Hosp.
Dyspnoea 3,539 13.7% 151 928
Wrong technique in device usage process 2,673 10.3% 1 75
Drug ineffective 2,522 9.7% 53 404
Product complaint 2,417 9.3% 3 75
Product dose omission issue 2,235 8.6% 18 209
Death 1,660 6.4% 1,634 147
Cough 1,520 5.9% 16 192
Asthma 1,275 4.9% 77 971
Hospitalisation 1,259 4.9% 40 1,257
Chronic obstructive pulmonary disease 1,145 4.4% 180 797
Pneumonia 1,064 4.1% 117 707
Dysphonia 943 3.6% 0 46
Product use in unapproved indication 735 2.8% 83 168
Condition aggravated 718 2.8% 160 262
Product dispensing error 692 2.7% 2 10

Other Indications for FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE

Product used for unknown indication (13,652) Chronic obstructive pulmonary disease (8,730) Asthma (2,468) Emphysema (377) Dyspnoea (290) Cough (96) Lung disorder (85) Bronchitis (81) Asthma-chronic obstructive pulmonary disease overlap syndrome (68) Lung neoplasm malignant (38)

Other Drugs Used for Pulmonary fibrosis

PIRFENIDONE (3,063) NINTEDANIB (1,539) RITUXIMAB (201) TREPROSTINIL (171) AMBRISENTAN (168) FLUTICASONE\SALMETEROL (148) UNSPECIFIED INGREDIENT (118) MYCOPHENOLATE MOFETIL (106) ALBUTEROL (62) PREDNISONE (54)

Related Pages

FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE Full Profile All Pulmonary fibrosis Drugs FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE Demographics FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE Timeline