Does CARBOXYMETHYLCELLULOSE Cause Recalled product? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Recalled product have been filed in association with CARBOXYMETHYLCELLULOSE (Rugby Carboxymethylcellulose Sodium 0.5% Eye Drops). This represents 0.3% of all adverse event reports for CARBOXYMETHYLCELLULOSE.
8
Reports of Recalled product with CARBOXYMETHYLCELLULOSE
0.3%
of all CARBOXYMETHYLCELLULOSE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Recalled product From CARBOXYMETHYLCELLULOSE?
Of the 8 reports, 1 (12.5%) resulted in death, 1 (12.5%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBOXYMETHYLCELLULOSE. However, 8 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 Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which CARBOXYMETHYLCELLULOSE Alternatives Have Lower Recalled product Risk?
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\GLYCERIN
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\GLYCERIN\POLYSORBATE 80
CARBOXYMETHYLCELLULOSE vs CARBOXYMETHYLCELLULOSE\HYPROMELLOSES
CARBOXYMETHYLCELLULOSE vs CARFENTANIL
CARBOXYMETHYLCELLULOSE vs CARFILZOMIB