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albuterol / ipratropium

A fixed combination of 2 drugs in one pill. Sold as Combivent.

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.

B

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 (77/100)

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

Safety: 88

Evidence: 57

Regulatory history: 68

Money & lawsuits: 100

Options: 70

Money and lawsuits

In 2024, drug companies reported $0 in payments to US physicians and hospitals tied to this combination's brands across 0 transactions.

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

381,509Medicare Part D patients (2024)
1,243,653prescriptions filled
$327average cost per fill
$406Mtotal Medicare spend
ProductFills$/fill
Ipratropium-Albuterol641,618$29
Combivent Respimat602,035$644

Questions to ask your prescriber

  1. This is a fixed combination of albuterol and ipratropium. Why both together, instead of only the one I need?
  2. The most-reported problems in FDA's adverse event data are dyspnoea, asthma, cough. How would we recognize and handle those?
  3. Why this one over bambuterol, bitolterol, clenbuterol? What would make you pick one of those instead?
  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 dyspnoea, asthma, cough, pneumonia. How would we recognize and handle those?