ATTENTION: Please enable Javascript in your browser for full site functionality.
Skip to navigation Skip to main content Skip to footer

Updates

SUB-TYPE:

Celebrating Pharmacy Innovation at the House of Commons

 

Alliance Healthcare celebrated the very best in pharmacy at the House of Lords as sponsors of the Innovation Awards at the Independent Pharmacy Awards.

 

Raj Nutan, Healthcare Strategy and Services Director, Alliance Healthcare and Sam Unsworth, Head of Communications, Alliance Healthcare had the honour to represent Alliance Healthcare at the prestigious setting, where Sam presented the award and said: “Innovation is essential to deliver the best service to patients. That’s why Alliance Healthcare is delighted to sponsor the Innovation Award at the Independent Pharmacy Awards.”

 

Deborah Evans, Remedi Health, Hampshire was our winner, who wowed the judges with her ability to not only lead but think outside the box.

 

Deborah has worked in pharmacy for over 35 years and runs a GpHC-registered private pharmacy which only opened last year. She has pulled together a brilliant team of 12 who have rolled out a range of private services for their patients – and in deciding not to provide NHS services, she has made a real success of her business in very tough times.

 

Her business model reverses the traditional community pharmacy approach. Instead of her predominately prescription and medicines business that offers services, hers is predominately a clinical service business of which medicines and prescriptions are part of the solution for the clients. The judges described Deborah as “an inspiration.”

 

Find out more about the awards here.

 

suicp

SUB-TYPE: COMPANY-LED RECALL

Company Led Recall - Endwarts freeze 7.5g

Viatris have informed that product Endwarts Freeze® has been manufactured with 5 tips instead of the stipulated 7 as indicated on the packaging and leaflet.

MHRA drug alert link: N/A   

PIP CODE

DESCRIPTION

SUPPLIER

AFFECTED BATCHES

4044368

ENDWARTS FREEZE 7.5g

VIATRIS UK HEALTHCARE

260222C08

 

Please return all affected stock to your original supplier for credit. Unfortunately we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies

Please note that anything not returned to us, or notified to us, within 3 months of this notification, cannot be reimbursed by way of a credit.

 

For more information please contact VIATRIS UK HEALTHCARE

 

Gary Marshall Gary.marshall@viatris.com 07817 486960

 

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 Medicines Defect Information: Flamingo Pharma UK Ltd, Ibuprofen 400mg Tablets, Paracetamol 500mg Tablets (Caplets)

 

Flamingo Pharma UK Ltd has identified an error relating to the ink printing of the batch number and expiry date on the carton for three batches of Ibuprofen 400mg Tablets. This notification includes all potentially impacted products/batches.

 

MHRA drug alert date:  12th October 2022

 

MHRA drug alert link: 

https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-flamingo-pharma-uk-ltd-ibuprofen-400mg-tablets-paracetamol-500mg-tablets-caplets-el-22-a-slash-43?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=ffbd7a57-60fc-4de6-afd0-d1d3fb960b3e&utm_content=immediately#download-document

 

Pip code

Product description

Supplier

Batch Numbers

ALLIANCE DO NOT STOCK

    IBUPROFEN 400MG TABLETS    

FLAMINGO PHARMA

20169

20170

20171

20172

20176

20177

20178

20179

20236

20237

20238

20239

20240

20241

20242

20243

20251

20252

20262

20263

20277

20278

20265

20266

20264

20279

20303

20304

20305

20306

20307

20314

20315

20316

20317

20318

20322

20323

20329

20355

20356

20357

20358

20359

20360

20361

20362

ALLIANCE DO NOT STOCKIBUPROFEN 400MG TABLETSFLAMINGO PHARMA

20103

20112

20257

20258

20259

20260

20261

20337

20338

20339

20340

20341

This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.

 

Further Information

For medical information and stock control queries please contact:

Flamingo Pharma

For medical information safety@flamingopharma.co.uk or general product enquiry sales@flamingopharma.co.uk +44 (0) 7733522465

Or

Mawdsley Brooks & Co Ltd

Overlabellingcustomerservices@mawdsleys.co.uk 01302 553064

 

Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.

SUB-TYPE: CLASS 2 RECALL

CLASS 2 RECALL - AMIODARONE HYDROCHLORIDE 50MG/ML SOLUTION FOR INJECTION/INFUSION

 

 

hameln pharma ltd is initiating a recall of batch 210505 of Amiodarone Hydrochloride 50 mg/ml Concentrate for Solution for Injection/Infusion as a precautionary measure. This is due to an increased presence of visible crystalline particles within the solution, identified during ongoing re-inspection of retained samples.

 

MHRA drug alert date: 11 October 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-hameln-pharma-ltd-amiodarone-hydrochloride-50-mg-slash-ml-concentrate-for-solution-for-injection-slash-infusion-el-22-a-slash-42?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=8736ec08-585b-4e2f-9985-026dc8594eef&utm_content=immediately

  Pip Code

     Product Description

 Supplier

Batch Numbers

ALLIANCE DO NOT STOCK

AMIODARONE HYDROCHLORIDE 50MG/ML

SOLUTION FOR INJECTION/INFUSION

 HAMELN PHARMA LTD

    210505

Alliance do not stock the above products so we will not be accepting Customer returns on this recall.

 

For more information or supply queries, please contact or email hameln pharma ltd customer services on +44 (0)1452 621 661 or customer.services@hameln-pharma.co.uk

For medical information queries, please contact or email hameln pharma ltd Medicines Information on +44 (0)1452 621 661 or drug.safety@hameln-pharma.co.uk

Please return all affected stock to your original supplier for credit. Unfortunately, we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.

SUB-TYPE: CLASS 2 RECALL

CLASS 2 RECALL - STEMETIL 5MG/5ML SYRUP

 

Sanofi is recalling all batches of the above product as a precautionary measure due to the identification of N-nitrosomethylphenylamine (NMPA) above the acceptable limit. Nitrosamines may increase the risk of cancer if people are exposed to them above acceptable levels and over long periods of time.

 

MHRA drug alert date: 10 October 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-aventis-pharma-limited-t-slash-a-sanofi-stemetil-5mg-slash-5ml-syrup-el-22-a-slash-41?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=8744b402-2664-40d4-a81b-0fbedeefc431&utm_content=immediately

  Pip Code

     Product Description

 Supplier

Batch Numbers

ALLIANCE DO NOT STOCK

STEMETIL SYRUP 5MG/5ML

 AVENTIS PHARM LTD (T/A SANOFI)

0032

0033

0034

0035

Alliance do not stock the above products so we will not be accepting Customer returns on this recall.

 

For stock control enquiries please contact:

GB-CustomerServices@sanofi.com

Phone number: 0800 854 430

 

For more information or medical information please contact:

uk-medicalinformation@sanofi.com

Phone number: 0800 035 25 25.

 

Please return all affected stock to your original supplier for credit. Unfortunately, we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.

SUB-TYPE:

Janssen Neuroscience RWA

 

We are pleased to announce that, as of 01 November 2022, Alliance Healthcare will become the only wholesaler to supply selected products from Janssen’s neuroscience product portfolio to all pharmacies, hospitals, and dispensing doctors in Great Britain. Supply to Northern Ireland is not included in this agreement.

 

A full list of the selected products is available here.

SUB-TYPE:

Some service disruption - 29 September 2022

 

Due to a network issue overnight which has since been fully resolved, there may be some disruption to service across our network (except Northern Ireland). Impacted customers are being contacted. We are sorry for any inconvenience caused.

 

Please contact Customer Service with any emergency requirements.

SUB-TYPE:

World Pharmacist Day 2022

 

World Pharmacist Day: Celebrating the changing face of modern pharmacy to create healthier futures

 

On Sunday 25 September we celebrated the International Pharmaceutical Federation’s (FIP) World Pharmacist Day 2022. As part of those celebrations, 27 pharmacists from across the globe and the AmerisourceBergen family, contributed to a digital book of celebration, which aims to highlight the changing role of pharmacists and how they can create healthier futures. 

 

The book, which was developed as part celebrations for the FIP World Pharmacist Day, which this year is focusing on “pharmacy united in action for a healthier world” - also highlights how pharmacists have a key role in creating a healthier world and keeping our communities fit and healthy. 

 

Read more...

SUB-TYPE: CLASS 2 RECALL

CLASS 2 RECALL - SANDIMMUN ORAL SOLUTION

 

 

Class 2 Recall -  Sandimmun Oral Solution

 

Novartis Pharmaceuticals UK are recalling the above batch due to the presence of crystals in the solution. The crystals have been identified as the active substance (ciclosporin). The presence of crystals has been observed in some finished product packs marketed in other countries that share the same master batch as the UK batch above. Therefore, this UK batch is recalled as a precautionary measure. Novartis Pharmaceuticals UK have confirmed no other batches of the product are impacted.

 

MHRA drug alert date: 20 September 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-novartis-pharmaceuticals-uk-sandimmun-oral-solution-el-22-a-slash-40?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=8bfa30ef-b0bd-4cf8-8ca4-e989982960bf&utm_content=immediately

 

  Pip Code

     Product Description

 Supplier

Batch Numbers

ALLIANCE DO NOT  STOCK

     SANDIMMUN ORAL  SOLUTION  

NOVARTIS PHARMACEUTICALS

  ADP326002

 

 

Alliance do not stock the above products so we will not be accepting Customer returns on this recall.

Further Information For more information, medical or supply enquiries. 

Please contact 01276 698370, or email medinfo.uk@novartis.com

 

 

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 Medicines Defect Information

Rosemont Pharmaceuticals Ltd. has made the MHRA aware that the expiry dates stamped on the base of the bottle are incorrect for 2 batches of Atorvastatin 4mg/ml Oral Suspension and 2 batches of Sildenafil 10mg/ml Oral Suspension.

 

MHRA drug alert date:  14 September 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-rosemont-pharmaceuticals-ltd-atorvastatin-4mg-slash-ml-oral-suspension-and-sildenafil-10mg-slash-ml-oral-suspension-el-22-a-slash-39

 

 

Pip code

Product description

Supplier

Batch Numbers

1256031

ATORVASTATIN ORAL SUSP 4MG/ML 150ML

ROSEMONT PHARMA

ATV21001

ATV21002

8045130SILDENAFIL SF ORAL SUSP 10MG/ML 122MLROSEMONT PHARMA
SLD22001
SLD22002

This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.

 

Further Information

For more information, medical or supply enquiries, please contact: pharmacovigilance@rosemontpharma.com

 

Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.