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JAMP Venlafaxine XR 37.5 mg (lot PTC5140A) sold to pharmacies in bottles of 100 capsules for dispensing.
Official notice
21 Jun 2023
Last checked
21 Jun 2023
An official Health Canada notice concerns JAMP Venlafaxine XR 37.5 mg (lot PTC5140A) sold to pharmacies in bottles of 100 capsules for dispensing.. Certain bottles of JAMP Venlafaxine XR 37.5 mg capsules recalled due to mislabelling that could lead to overdose Published 2023-06-21.
What to do now
Check the capsules in your pharmacy bottle of JAMP Venlafaxine XR 37. 5 mg capsules to make sure it contains 37. 5 mg capsules (grey / pink in colour) and not 150 mg capsules (caramel in colour). If you are unsure, contact your pharmacist to check if your bottle contains the correct capsules. If you see incorrect capsules, stop taking the medication and contact your pharmacy immediately for a replacement product. Return the affected product to your pharmacy for proper disposal. Contact your health care professional if you have taken the wrong dose of your medication. Seek medical attention immediately if you experience any serious side effects from Venlafaxine XR, which may include allergic reactions, gastrointestinal bleeding, seizures, heart rhythm problems, blurred vision, eye pain, or severe headache. Contact JAMP Pharma Corporation by email at alewicki@jamppharma. Com if you have questions about this recall. Report any health product-related side effects or complaints to Health Canada.
Recall number
73862
Official notice
2023-06-21
The hazard
The hazard
Certain bottles of JAMP Venlafaxine XR 37.5 mg capsules recalled due to mislabelling that could lead to overdose
How to check if you're affected
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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Where it was sold
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Company & contacts
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Brand: Jamp Venlafaxine Xr 37.5 MG Sold To Pharmacies In Bottles Of 100 Capsules For Dispensing.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
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