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Dobutamine (Dobutamine) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Dobutamine and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (2)

Reports by Reaction Type

Cardiogenic Shock (2)Eosinophilic Myocarditis (1)

Possible Dobutamine side effects in 73 year old female

Reported by a health professional (non-physician/pharmacist) from Germany on 2012-08-02

Patient: 73 year old female

Reactions: Cardiogenic Shock

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Dobutamine
    Indication: Septic Shock

Dopamine HCL
    Indication: Septic Shock

Nitroglycerin
    Indication: Angina Pectoris



Possible Dobutamine side effects in 46 year old male

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-30

Patient: 46 year old male

Reactions: Eosinophilic Myocarditis, Cardiogenic Shock

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Acetaminophen and Tramadol HCL
    Dosage: unk
    Administration route: Oral
    Indication: Pain
    End date: 2012-07-01

Aldactone
    Dosage: 50 mg, daily
    Administration route: Oral
    End date: 2012-07-01

Bisoprolol Fumarate
    Dosage: 2.5 mg, daily
    Administration route: Oral
    End date: 2012-07-01

Corotrope
    Dosage: unk
    Indication: Ejection Fraction Decreased
    Start date: 2012-06-06
    End date: 2012-07-01

Dobutamine
    Dosage: unk
    Indication: Ejection Fraction Decreased
    Start date: 2012-06-06

Imovane
    Dosage: unk
    Administration route: Oral
    End date: 2012-07-01

Lasix
    Dosage: 40 mg, daily
    Administration route: Oral
    End date: 2012-07-01

Procoralan
    Dosage: 7.5 mg, 2x/day
    Administration route: Oral
    End date: 2012-07-01

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