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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 SERETIDE Cause Product quality issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product quality issue have been filed in association with SERETIDE. This represents 5.4% of all adverse event reports for SERETIDE.

14
Reports of Product quality issue with SERETIDE
5.4%
of all SERETIDE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product quality issue From SERETIDE?

Of the 14 reports, 5 (35.7%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SERETIDE. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does SERETIDE Cause?

Death (39) Dyspnoea (20) Cough (16) Angioedema (15) Asthmatic crisis (15) Drug ineffective (15) Fatigue (15) Pneumonia (11) Lobar pneumonia (9) Pulmonary fibrosis (9)

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 SERETIDE Alternatives Have Lower Product quality issue Risk?

SERETIDE vs SEROQUEL SERETIDE vs SERTRALINE SERETIDE vs SETMELANOTIDE SERETIDE vs SEVELAMER SERETIDE vs SEVOFLURANE

Related Pages

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