Does NEOSTIGMINE Cause Product quality issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product quality issue have been filed in association with NEOSTIGMINE. This represents 2.0% of all adverse event reports for NEOSTIGMINE.
5
Reports of Product quality issue with NEOSTIGMINE
2.0%
of all NEOSTIGMINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product quality issue From NEOSTIGMINE?
Of the 5 reports, 1 (20.0%) required hospitalization, and 3 (60.0%) 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 NEOSTIGMINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does NEOSTIGMINE Cause?
Cardiac arrest (23)
Hypotension (21)
Bradycardia (20)
Drug ineffective (20)
Exposure during pregnancy (17)
Off label use (15)
Foetal exposure during pregnancy (12)
Atrioventricular block complete (10)
Maternal exposure during pregnancy (10)
Product use in unapproved indication (10)
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 NEOSTIGMINE Alternatives Have Lower Product quality issue Risk?
NEOSTIGMINE vs NEOSTIGMINE METHYLSULFATE
NEOSTIGMINE vs NEPAFENAC
NEOSTIGMINE vs NERATINIB
NEOSTIGMINE vs NETARSUDIL
NEOSTIGMINE vs NETUPITANT\PALONOSETRON