Product description
Valpam 5mg tablets are used to treat anxiety disorders, alcohol withdrawal symptoms and muscle spasms.
AUST R 80811
All batches
AUST R 80811
All batches
See a list of details to help identify the product
Reason the product is recalled
Blister pack sheets containing other medicines may have been substituted into some packs of Valpam 5mg tablets. These medicines may include (but may not be limited to) Amlodipine Sandoz 5mg tablets.
The hazards to consumers
If a patient has an affected pack, there is a risk that they will not have an adequate supply of their medicine and could take the incorrect medicine, which could have serious health consequences.
What consumers should do
If you or someone you provide care for takes Valpam 5 (diazepam) 5mg tablets supplied in 50 tablet blister packs, do not take them and please promptly return any unused medicine to a pharmacy for a refund. If possible, you are advised to return your Valpam 5 to the same pharmacy from which it was dispensed.
There are a number of generic diazepam products that are bioequivalent to Valpam 5. They contain the same active ingredient and work in the same way and in most situations can be safely substituted for any returned Valpam 5. If you have a valid prescription (this includes repeat prescriptions), the pharmacist will be able to provide you with an equivalent alternative.
Please note that all tablets or capsules supplied in a pack should be identical and any product names on the blister pack should match those on the external packaging. If you notice any discrepancies with your medicine, talk to your pharmacist.
If you have any questions or concerns about this issue, talk to your health professional.
There are a number of generic diazepam products that are bioequivalent to Valpam 5. They contain the same active ingredient and work in the same way and in most situations can be safely substituted for any returned Valpam 5. If you have a valid prescription (this includes repeat prescriptions), the pharmacist will be able to provide you with an equivalent alternative.
Please note that all tablets or capsules supplied in a pack should be identical and any product names on the blister pack should match those on the external packaging. If you notice any discrepancies with your medicine, talk to your pharmacist.
If you have any questions or concerns about this issue, talk to your health professional.
Details to help identify the product
Supplier running the recall
Arrow Pharma Pty Ltd
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2017/16139 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.