Does ACLIDINIUM Cause Product quality issue? 557 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 557 reports of Product quality issue have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 11.2% of all adverse event reports for ACLIDINIUM.
557
Reports of Product quality issue with ACLIDINIUM
11.2%
of all ACLIDINIUM reports
3
Deaths
81
Hospitalizations
How Dangerous Is Product quality issue From ACLIDINIUM?
Of the 557 reports, 3 (0.5%) resulted in death, 81 (14.5%) required hospitalization, and 3 (0.5%) 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 ACLIDINIUM. However, 557 reports have been filed with the FAERS database.
What Other Side Effects Does ACLIDINIUM Cause?
Dyspnoea (1,706)
Device malfunction (1,325)
Drug dose omission (996)
Asthma (857)
Intentional product misuse (745)
Chronic obstructive pulmonary disease (697)
Wheezing (688)
Off label use (620)
Device issue (499)
Cough (471)
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 ACLIDINIUM Alternatives Have Lower Product quality issue Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL