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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 DEVICE Cause Cerebrovascular accident? 129 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Cerebrovascular accident have been filed in association with DEVICE. This represents 1.0% of all adverse event reports for DEVICE.

129
Reports of Cerebrovascular accident with DEVICE
1.0%
of all DEVICE reports
13
Deaths
40
Hospitalizations

How Dangerous Is Cerebrovascular accident From DEVICE?

Of the 129 reports, 13 (10.1%) resulted in death, 40 (31.0%) required hospitalization, and 7 (5.4%) were considered life-threatening.

Is Cerebrovascular accident Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 129 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE Cause?

Blood glucose increased (2,114) Device issue (1,417) Product use issue (1,076) Intercepted product preparation error (1,033) Wrong technique in product usage process (935) Device leakage (795) Injection site pain (751) Syringe issue (634) Product quality issue (567) Drug ineffective (488)

What Other Drugs Cause Cerebrovascular accident?

ROSIGLITAZONE (7,899) APIXABAN (7,237) RIVAROXABAN (4,111) ADALIMUMAB (2,756) LENALIDOMIDE (2,330) DABIGATRAN ETEXILATE (2,175) TESTOSTERONE (2,172) ASPIRIN (1,904) SACUBITRIL\VALSARTAN (1,864) INSULIN GLARGINE (1,805)

Which DEVICE Alternatives Have Lower Cerebrovascular accident Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

DEVICE Full Profile All Cerebrovascular accident Reports All Drugs Causing Cerebrovascular accident DEVICE Demographics