Does BOTULINUM TOXIN TYPE A Cause Angina pectoris? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Angina pectoris have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 0.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
17
Reports of Angina pectoris with BOTULINUM TOXIN TYPE A
0.5%
of all BOTULINUM TOXIN TYPE A reports
1
Deaths
16
Hospitalizations
How Dangerous Is Angina pectoris From BOTULINUM TOXIN TYPE A?
Of the 17 reports, 1 (5.9%) resulted in death, 16 (94.1%) required hospitalization.
Is Angina pectoris Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does BOTULINUM TOXIN TYPE A Cause?
Off label use (1,785)
Drug ineffective (1,175)
Drug intolerance (1,004)
Product use in unapproved indication (950)
Headache (797)
Migraine (775)
Maternal exposure during pregnancy (716)
Pain (714)
Hypoaesthesia (703)
Nausea (665)
What Other Drugs Cause Angina pectoris?
ASPIRIN (706)
ROSIGLITAZONE (680)
RANOLAZINE (583)
ATORVASTATIN (559)
AMLODIPINE (509)
RITUXIMAB (502)
CLOPIDOGREL BISULFATE (471)
SACUBITRIL\VALSARTAN (468)
PREDNISONE (462)
METFORMIN (452)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Angina pectoris Risk?
BOTULINUM TOXIN TYPE A vs BREMELANOTIDE
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB VEDOTIN
BOTULINUM TOXIN TYPE A vs BREO ELLIPTA
BOTULINUM TOXIN TYPE A vs BREXANOLONE