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side effects patient, 81 years of age, weighting 179.9 lb, was diagnosed with parkinson's disease and took Bromergon (bromocriptine) tablet 2.5 Mg, Once/single, Or. View more Serious Adverse Events reported to FDA.

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List of Bromergon (bromocriptine) Tablet Adverse Effects reported to US Food and Drug Administration (FDA)

Cerebrovascular Accident, Convulsion, Loss Of Consciousness (5842900-1)
on Aug 04, 2008 Male patient from UNITED STATES , 81 years of age, weighting 179.9 lb, was diagnosed with
  • parkinson's disease
and was treated with Bromergon (bromocriptine) Tablet. Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, convulsion, loss of consciousness. Bromergon (bromocriptine) Tablet dosage: 2.5 Mg, Once/single, Oral.
Patient also using the following medications:
  • Propranolol
  • Sanctura
  • Aspirin
Patient was hospitalized.

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Bromergon (bromocriptine) Tablet Information

More About Bromergon (bromocriptine) tablet

Side Effects reported to FDA: 1. View FDA Adverse Reports

Bromergon (bromocriptine) Tablet safety alerts: No

Reported hospitalizations: 1

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Bromergon (bromocriptine) Tablet Adverse Reactions

Cerebrovascular Accident ( 1 Reports)

Convulsion ( 1 Reports)

Loss Of Consciousness ( 1 Reports)

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