Dobutamine Side Effects
Medically reviewed by Drugs.com. Last updated on Sep 23, 2023.
Applies to dobutamine: intravenous solution.
Serious side effects of Dobutamine
Along with its needed effects, dobutamine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor or nurse immediately if any of the following side effects occur while taking dobutamine:
More common
- Dizziness
- headache
- increased heart rate
- numbness or tingling in the arms or legs
- trouble thinking, speaking, or walking
- weakness
Less common
- Chest pain
- fast, irregular, pounding, or racing heartbeat or pulse
- trouble breathing
Incidence not known
- Back, tarry stools
- bluish color
- blurred vision
- changes in skin color
- chest discomfort or tightness
- chills
- confusion
- cough
- difficulty swallowing
- dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position
- fever
- hives, itching, skin rash
- painful or difficult urination
- puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
- sore throat
- sores, ulcers, or white spots on the lips or in the mouth
- sweating
- swelling of the fingers, hands, feet, or lower legs
- swollen glands
- unusual bleeding or bruising
- weight gain
Other side effects of Dobutamine
Some side effects of dobutamine may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
Less common
For Healthcare Professionals
Applies to dobutamine: intravenous solution.
General
The most common adverse reaction was heart rate increased by 30 beats per minute or more.[Ref]
Cardiovascular
Very common (10% or more): Heart rate increased by 30 beats per minute (bpm) or more (10%)
Common (1% to 10%): Systolic blood pressure increased by 50 mmHg or more, premature ventricular beats increased, anginal pain, palpitations, blood pressure decreased, ventricular dysrhythmia, dose-dependent ventricular extrasystoles, ventricular frequency increased in patients with atrial fibrillation, vasoconstriction in patients previously treated with beta blockers, supraventricular extrasystoles, ventricular tachycardia
Uncommon (0.1% to 1%): Ventricular fibrillation
Very rare (less than 0.01%): Bradycardia, myocardial ischemia, myocardial infarction, cardiac arrest, second degree atrioventricular block, coronary vasospasms, hypertensive/hypotensive blood pressure decompensation, intracavitary pressure gradients
Frequency not reported: Systolic blood pressure increased by 10 to 20 mmHg, heart rate increased by 5 to 15 bpm, blood pressure decreased precipitously, pulmonary capillary pressure decreased, pectoral anginal discomfort, stress cardiomyopathy, eosinophilic myocarditis, fatal cardiac rupture[Ref]
Dermatologic
Common (1% to 10%): Exanthema, skin rash
Very rare (less than 0.01%): Petechial bleeding
Frequency not reported: Pruritus of the scalp[Ref]
Local
Common (1% to 10%): Phlebitis, inflammation
Very rare (less than 0.01%): Cutaneous necrosis[Ref]
Hematologic
Common (1% to 10%): Eosinophilia, thrombocyte aggregation inhibited when continuing infusion over a number of days
Frequency not reported: Thrombocytopenia[Ref]
Other
Common (1% to 10%): Nonspecific chest pain, fever
Frequency not reported: Feeling of heat and anxiety[Ref]
Respiratory
Common (1% to 10%): Shortness of breath, bronchospasm[Ref]
Nervous system
Common (1% to 10%): Headache
Frequency not reported: Paresthesia, tremor[Ref]
Genitourinary
Common (1% to 10%): Urgency increased at high doses of infusion
Frequency not reported: Urinary urgency[Ref]
Gastrointestinal
Common (1% to 10%): Nausea[Ref]
Metabolic
Very rare (less than 0.01%): Hypokalemia
Frequency not reported: Serum potassium decreased[Ref]
Immunologic
Frequency not reported: Hypersensitivity[Ref]
Musculoskeletal
Frequency not reported: Myoclonic spasm[Ref]
Psychiatric
Frequency not reported: Restlessness, anxiety[Ref]
More about dobutamine
- Check interactions
- Compare alternatives
- Pricing & coupons
- Reviews (1)
- Dosage information
- During pregnancy
- Drug class: cardiac stressing agents
- Breastfeeding
- En español
Patient resources
Other brands
Professional resources
Related treatment guides
References
1. Product Information. Dobutrex (dobutamine). Lilly, Eli and Company. 2002;PROD.
2. Cerner Multum, Inc. UK Summary of Product Characteristics.
3. Cerner Multum, Inc. Australian Product Information.
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.