Xenadrine Reviews

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Summary

Xenadrine is a supplement business that sells four products, including Core Hardcore Thermogenic, Maximum Hardcore Xenadrine Ripped, Powerful and Ultimate. RiskScore has not tested its products yet. The FDA has received 18 adverse event reports submitted to the FDA covering the years 2004 to 2018.

Public safety signals

18 adverse event reports in public records.

  • Adverse eventSource: openFDA

    Adverse event report: Cardiac failure, Cardiomyopathy

    Product: XENADRINE. Outcome: Life Threatening, Hospitalization, Disability, Visited a Health Care Provider. Reactions: Cardiac failure, Cardiomyopathy. FDA CAERS report 2018-CFS-003589.

  • Adverse eventSource: openFDA

    Adverse event report: Heart rate increased, Insomnia, Supraventricular tachycardia

    Product: XENADRINE CAPSULES (DIETARY SUPPLEMENT) CAPSULE. Outcome: Other Serious or Important Medical Event, Visited Emergency Room. Reactions: Heart rate increased, Insomnia, Supraventricular tachycardia. FDA CAERS report 184660.

  • Adverse eventSource: openFDA

    Adverse event report: Diarrhoea, Hepatic enzyme increased, Skin odour abnormal

    Product: XENADRINE CAPSULES DIETARY SUPPLEMENT CAPSULE. Outcome: Other Serious or Important Medical Event, Visited a Health Care Provider. Reactions: Diarrhoea, Hepatic enzyme increased, Skin odour abnormal. FDA CAERS report 181547.

  • Adverse eventSource: openFDA

    Adverse event report: Fibrocystic breast disease

    Product: XENADRINE CAPSULES. Outcome: Other Serious or Important Medical Event. Reactions: Fibrocystic breast disease. FDA CAERS report 172593.

  • Adverse eventSource: openFDA

    Adverse event report: Abdominal pain, Chromaturia, Decreased appetite and 6 more

    Product: XENADRINE. Outcome: Hospitalization, Other Serious or Important Medical Event, Visited Emergency Room, Visited a Health Care Provider. Reactions: Abdominal pain, Chromaturia, Decreased appetite, Fatigue, Hepatitis a, Liver function test abnormal, Nausea, Pruritus, Vomiting. FDA CAERS report 150602.

  • Adverse eventSource: openFDA

    Adverse event report: Diarrhoea, Headache, Pain and 4 more

    Product: XENADRINE ULTRA. Outcome: Other Serious or Important Medical Event. Reactions: Diarrhoea, Headache, Pain, Psychomotor skills impaired, Speech disorder, Visual acuity reduced, Vomiting. FDA CAERS report 128938.

  • Adverse eventSource: openFDA

    Adverse event report: Headache, Subarachnoid haemorrhage

    Product: XENADRINE. Outcome: Life Threatening, Hospitalization, Visited Emergency Room. Reactions: Headache, Subarachnoid haemorrhage. FDA CAERS report 128539.

  • Adverse eventSource: openFDA

    Adverse event report: Headache

    Product: XENADRINE ULTRA RAPID RELEASE. Outcome: Other Serious or Important Medical Event, Visited Emergency Room. Reactions: Headache. FDA CAERS report 124339.

  • Adverse eventSource: openFDA

    Adverse event report: Hepatic enzyme increased, Jaundice, Liver injury and 1 more

    Product: XENADRINE. Outcome: Hospitalization. Reactions: Hepatic enzyme increased, Jaundice, Liver injury, Malaise. FDA CAERS report 118518.

  • Adverse eventSource: openFDA

    Adverse event report: Asthenia, Dyspnoea, Fatigue and 3 more

    Product: XENADRINE. Outcome: Life Threatening, Disability, Other Serious or Important Medical Event. Reactions: Asthenia, Dyspnoea, Fatigue, Irritability, Pain, Tremor. FDA CAERS report 90080.

Show 8 more
  • Adverse eventSource: openFDA

    Adverse event report: Chest discomfort, Dyspnoea

    Product: XENADRINE. Outcome: Hospitalization. Reactions: Chest discomfort, Dyspnoea. FDA CAERS report 86368.

  • Adverse eventSource: openFDA

    Adverse event report: Death, Pulse absent, Respiratory arrest

    Product: XENADRINE. Outcome: Death, Visited Emergency Room. Reactions: Death, Pulse absent, Respiratory arrest. FDA CAERS report 71305.

  • Adverse eventSource: openFDA

    Adverse event report: Convulsion, Emergency care examination, Physical examination

    Product: XENADRINE. Outcome: Hospitalization, Visited a Health Care Provider. Reactions: Convulsion, Emergency care examination, Physical examination. FDA CAERS report 71275.

  • Adverse eventSource: openFDA

    Adverse event report: Hemiparesis, Hospitalisation, Paraesthesia

    Product: XENADRINE. Outcome: Hospitalization. Reactions: Hemiparesis, Hospitalisation, Paraesthesia. FDA CAERS report 70056.

  • Adverse eventSource: openFDA

    Adverse event report: Asthenia, Asthma, Disorientation and 6 more

    Product: XENADRINE. Outcome: Life Threatening, Visited Emergency Room, Visited a Health Care Provider. Reactions: Asthenia, Asthma, Disorientation, Emergency care examination, Headache, Hypertension, Respiratory arrest, Rhinitis, Weight decreased. FDA CAERS report 66814.

  • Adverse eventSource: openFDA

    Adverse event report: Abdominal pain, Alanine aminotransferase increased, Aspartate aminotransferase increased and 2 more

    Product: XENADRINE. Outcome: Hospitalization. Reactions: Abdominal pain, Alanine aminotransferase increased, Aspartate aminotransferase increased, Cholelithiasis obstructive, Jaundice. FDA CAERS report 66169.

  • Adverse eventSource: openFDA

    Adverse event report: Blood potassium decreased, Chest pain, Dyspnoea and 4 more

    Product: XENADRINE. Outcome: Life Threatening, Hospitalization, Required Intervention, Visited Emergency Room. Reactions: Blood potassium decreased, Chest pain, Dyspnoea, Fatigue, Hospitalisation, Myocardial infarction, Palpitations. FDA CAERS report 65679.

  • Adverse eventSource: openFDA

    Adverse event report: Headache, Pain, Tenderness

    Product: XENADRINE. Outcome: Other Outcome. Reactions: Headache, Pain, Tenderness. FDA CAERS report 65433.

Products

4 products listed for Xenadrine.

ProductRating
Core Hardcore Thermogenic
Not tested yet
Maximum Hardcore Xenadrine Ripped
Not tested yet
Powerful
Not tested yet
Ultimate
Not tested yet

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