Drug Guide
Carbidopa; Levodopa
Classification
Therapeutic: Antiparkinsonian agent
Pharmacological: Dopamine precursor and decarboxylase inhibitor combination
FDA Approved Indications
- Parkinson's disease
- Parkinsonian syndromes
Mechanism of Action
Levodopa is converted to dopamine in the brain, replenishing dopamine levels. Carbidopa inhibits peripheral decarboxylation of levodopa, increasing central nervous system availability and reducing peripheral side effects.
Dosage and Administration
Adult: Dosage varies based on form and response; typically, 25/100 mg three times daily, adjusted according to clinical response.
Pediatric: Not approved for use in children; safety and efficacy not established.
Geriatric: Start low and titrate gradually; monitor for side effects.
Renal Impairment: Adjust dosage as needed, especially in severe impairment.
Hepatic Impairment: Use with caution; monitor liver function.
Pharmacokinetics
Absorption: Rapid absorption from gastrointestinal tract.
Distribution: Widely distributed in body tissues.
Metabolism: Levodopa metabolized in the peripheral tissues and liver; carbidopa inhibits peripheral decarboxylation of levodopa.
Excretion: Primarily in urine, as metabolites.
Half Life: Levodopa: approximately 1-2 hours; extended-release formulations vary.
Contraindications
- Narrow-angle glaucoma
- History of melanoma
Precautions
- Psychosis, history of melanoma, cardiovascular disease, concurrent use with non-selective MAO inhibitors, orthostatic hypotension, glaucoma, vitamin B6 deficiency.
Adverse Reactions - Common
- Nausea (Very common)
- Dizziness (Common)
- Orthostatic hypotension (Common)
- Dyskinesias (Common)
Adverse Reactions - Serious
- Neuroleptic malignant syndrome (Rare)
- Psychosis (Uncommon)
- Hepatotoxicity (Rare)
- Severe dyskinesias or movements (Uncommon)
Drug-Drug Interactions
- MAO inhibitors, antipsychotics, iron supplements, pyridoxine (vitamin B6), certain antidepressants
Drug-Food Interactions
- High-protein meals may reduce absorption
Drug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for therapeutic response and side effects, including dyskinesias, orthostatic hypotension, mood changes.
Diagnoses:
- Risk for falls
- Impaired physical mobility
- Imbalanced nutrition
Implementation: Administer with food if GI upset occurs, but avoid high-protein meals close to dosing.
Evaluation: Assess improvement in motor symptoms, monitor for adverse reactions.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Do not stop abruptly.
- Report any hallucinations, unusual movements, or severe side effects.
- Avoid high-protein meals around dosing times.
Special Considerations
Black Box Warnings:
- Potential for melanoma; educate patients to monitor skin and report any changes.
Genetic Factors: Patients with genetic predisposition to melanoma should be closely monitored.
Lab Test Interference: May affect certain lab tests, including those for phenylketonuria.
Overdose Management
Signs/Symptoms: Dyskinesias, hallucinations, hypotension, nausea, vomiting.
Treatment: Supportive care, monitor vital signs, gastric lavage if indicated, and symptomatic treatment.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F).
Stability: Stable under recommended conditions; check expiration date regularly.