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No image published for this recall

Valpam 5 (diazepam) 5mg tablets in 50 tablet blister packs

Official notice

10 Jun 2017

Last checked

10 Jun 2017

Risk not stated by sourceACCC

An official ACCC notice concerns Valpam 5 (diazepam) 5mg tablets in 50 tablet blister packs. 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. Published 2017-06-10.

What to do now

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.

Recall number

66a60fa9-e48f-428e-b19b-795df4dd8022

Official notice

2017-06-10

The hazard

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.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

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Affected products

Product 1

Valpam 5mg tablets are used to treat anxiety disorders, alcohol withdrawal symptoms and muscle spasms. AUST R 80811 All batches

Risk / hazard

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.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

AU · Australia

Affected area 1

AU · Australia

Source & status

Source

Tier

beta

Category

HOME

Classification

Pharmacy and medical products

App estimate

unspecified

Recall details

Recall number

66a60fa9-e48f-428e-b19b-795df4dd8022

Classification

Pharmacy and medical products

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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