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carbidopa / levodopa

A fixed combination of 2 drugs in one pill. Sold as Crexont, Dhivy, Duopa, Rytary, Sinemet and 1 more.

A combination is graded by its riskiest ingredient: each part of the score is the lowest of the ingredients' scores. This grade answers one narrow question: how strong is the public evidence and safety record behind this drug, and how clean is its money trail and court record? It is not a verdict on whether the drug is right for you.

C

What is in it

Each ingredient has its own full page with the FDA label, side-effect reports, recalls, evidence, and payments. Open them for the detail behind this grade.

Score breakdown (73/100)

Safety ×35%
A
Evidence ×25%
D
Regulatory ×15%
A
Money & lawsuits ×15%
C
Options ×10%
F

Safety: 89

Evidence: 52

Regulatory history: 96

Money & lawsuits: 70

Options: 40

Money and lawsuits

In 2024, drug companies reported $1,581,918 in payments to US physicians and hospitals tied to this combination's brands across 17,797 transactions (Crexont $537,294, Rytary $495,870, Duopa $308,253, Vyalev $240,266, Dhivy $237).

No pending federal MDL names this combination or its brands.

The ingredients' own payments and lawsuits are on their pages and already count toward this grade.

Who takes it and what it costs

738,372Medicare Part D patients (2024)
3,799,983prescriptions filled
$105average cost per fill
$400Mtotal Medicare spend
ProductFills$/fill
Carbidopa-Levodopa2,964,396$31
Carbidopa-Levodopa ER604,966$50
Rytary224,759$1,209
Crexont2,918$854
Dhivy1,703$575
Sinemet844$364
Duopa397$7,017

Questions to ask your prescriber

  1. This is a fixed combination of carbidopa and levodopa. Why both together, instead of only the one I need?
  2. In 2026 the FDA issued a safety communication about this drug (FDA Is Requiring Warning about Vitamin B6 Deficiency and Associated Seizures for Drug Products Containing Carb). Does that risk apply to me?
  3. The most-reported problems in FDA's adverse event data are hallucination, death, fall. How would we recognize and handle those?
  4. What result are we expecting, by when, and what is the plan if it does not happen?
  5. If 100 people like me took this drug, how many would actually get better because of it, and how many would be harmed by it? (Doctors call these the number needed to treat and the number needed to harm.)
  6. The most-reported problems in FDA's adverse event data are cough, parkinson^s disease, dyskinesia. How would we recognize and handle those?
  7. There is no generic. Is there an older generic in the same class that works as well for my situation?