Product description
Posicor (mibefradil Dihydrochloride) Tablets. 59510 (100mg) And 59511 (50mg). All Batches.
See a list of details to help identify the product
Reason the product is recalled
The Combination Of Posicor And Some Other Commonly Used Drugs, Among Them Cardiovascular Agents, May Increase The Side-effects Of These Other Medications.
The hazards to consumers
Adverse Reaction
What consumers should do
Patients Who Have Been Prescribed Posicor Should Not Discontinue Their Medication, But Should Contact Their Doctor Promptly. Any Queries To Tollfree Info Line 1800 771 444.
Details to help identify the product
Supplier running the recall
Roche Products Pty Limited
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 1998/3556 when contacting a regulator about this recall.
Recall and remedy questions
Contact the Therapeutic Goods Administration if you have:
- a question about the remedy being offered to you by the business that is responsible for managing this recall, or
- concerns about the way the business is managing this recall.