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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 BRIMONIDINE Cause Wrong technique in product usage process? 91 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Wrong technique in product usage process have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.8% of all adverse event reports for BRIMONIDINE.

91
Reports of Wrong technique in product usage process with BRIMONIDINE
0.8%
of all BRIMONIDINE reports
1
Deaths
0
Hospitalizations

How Dangerous Is Wrong technique in product usage process From BRIMONIDINE?

Of the 91 reports, 1 (1.1%) resulted in death.

Is Wrong technique in product usage process Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 91 reports have been filed with the FAERS database.

What Other Side Effects Does BRIMONIDINE Cause?

Treatment failure (2,849) Drug ineffective (1,402) Eye irritation (950) Ocular hyperaemia (917) Hypersensitivity (629) Erythema (604) Eye pain (560) Vision blurred (542) Headache (492) Dry eye (490)

What Other Drugs Cause Wrong technique in product usage process?

EVOLOCUMAB (21,664) ALBUTEROL (17,114) ADALIMUMAB (11,766) PEGFILGRASTIM (10,217) ETANERCEPT (9,835) ERENUMAB-AOOE (9,359) SACUBITRIL\VALSARTAN (8,022) LEUPROLIDE (5,062) FENTANYL (2,812) SEMAGLUTIDE (2,538)

Which BRIMONIDINE Alternatives Have Lower Wrong technique in product usage process Risk?

BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE BRIMONIDINE vs BRIMONIDINE\TIMOLOL BRIMONIDINE vs BRINTELLIX BRIMONIDINE vs BRINZOLAMIDE BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL

Related Pages

BRIMONIDINE Full Profile All Wrong technique in product usage process Reports All Drugs Causing Wrong technique in product usage process BRIMONIDINE Demographics