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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 SPIRIVA Cause Product quality issue? 621 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 621 reports of Product quality issue have been filed in association with SPIRIVA. This represents 17.9% of all adverse event reports for SPIRIVA.

621
Reports of Product quality issue with SPIRIVA
17.9%
of all SPIRIVA reports
0
Deaths
70
Hospitalizations

How Dangerous Is Product quality issue From SPIRIVA?

Of the 621 reports, 70 (11.3%) required hospitalization, and 1 (0.2%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPIRIVA. However, 621 reports have been filed with the FAERS database.

What Other Side Effects Does SPIRIVA Cause?

Incorrect route of drug administration (1,554) Dyspnoea (485) Off label use (292) Drug ineffective (240) Pneumonia (134) Cough (124) Chronic obstructive pulmonary disease (122) Dry mouth (72) Dysphonia (62) Lung neoplasm malignant (48)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which SPIRIVA Alternatives Have Lower Product quality issue Risk?

SPIRIVA vs SPIRONOLACTONE SPIRIVA vs SPRYCEL SPIRIVA vs STALEVO SPIRIVA vs STANNOUS FLUORIDE SPIRIVA vs STANOZOLOL

Related Pages

SPIRIVA Full Profile All Product quality issue Reports All Drugs Causing Product quality issue SPIRIVA Demographics