Does CARBOXYMETHYLCELLULOSE Cause Product use complaint? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product use complaint have been filed in association with CARBOXYMETHYLCELLULOSE (Rugby Carboxymethylcellulose Sodium 0.5% Eye Drops). This represents 0.7% of all adverse event reports for CARBOXYMETHYLCELLULOSE.
16
Reports of Product use complaint with CARBOXYMETHYLCELLULOSE
0.7%
of all CARBOXYMETHYLCELLULOSE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product use complaint From CARBOXYMETHYLCELLULOSE?
Of the 16 reports, 4 (25.0%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBOXYMETHYLCELLULOSE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does CARBOXYMETHYLCELLULOSE Cause?
Drug ineffective (903)
Macular degeneration (828)
Cataract (322)
Off label use (272)
Eye irritation (269)
Nausea (235)
Pain (221)
Therapeutic product effect incomplete (219)
Malaise (216)
Weight decreased (213)
What Other Drugs Cause Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which CARBOXYMETHYLCELLULOSE Alternatives Have Lower Product use complaint Risk?
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\GLYCERIN
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\GLYCERIN\POLYSORBATE 80
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\HYPROMELLOSES
CARBOXYMETHYLCELLULOSE vs CARFENTANIL
CARBOXYMETHYLCELLULOSE vs CARFILZOMIB