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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 METHYLCELLULOSE Cause Incorrect product administration duration? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product administration duration have been filed in association with METHYLCELLULOSE (CITRUCEL). This represents 14.7% of all adverse event reports for METHYLCELLULOSE.

14
Reports of Incorrect product administration duration with METHYLCELLULOSE
14.7%
of all METHYLCELLULOSE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Incorrect product administration duration From METHYLCELLULOSE?

Of the 14 reports.

Is Incorrect product administration duration Listed in the Official Label?

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

What Other Side Effects Does METHYLCELLULOSE Cause?

Off label use (18) Drug ineffective (16) Product complaint (13) Product use in unapproved indication (13) Diabetes mellitus (11) Dyspnoea (11) Rectal haemorrhage (11) Constipation (10) Abdominal pain (9) Choking (9)

What Other Drugs Cause Incorrect product administration duration?

ETONOGESTREL (3,974) POLYETHYLENE GLYCOL 3350 (2,129) NIRMATRELVIR\RITONAVIR (744) DOCOSANOL (634) LANSOPRAZOLE (564) LOPERAMIDE (543) NAPROXEN (499) INSULIN LISPRO (479) DICLOFENAC (362) OMEPRAZOLE (302)

Related Pages

METHYLCELLULOSE Full Profile All Incorrect product administration duration Reports All Drugs Causing Incorrect product administration duration METHYLCELLULOSE Demographics