Month: October 2022
WHO Global Alert on Contaminated Pediatrics Cough Syrups Identified In Gambia-West Africa
Drug Safety Alert
Update from WHO Global Surveillance and Monitoring System
| Date: | 12th of October 2022. |
| Target Audience: | • Healthcare Professionals- Physicians, Pharmacists, and Nurses. • Manufacturers and Importers of Glycerin containing formulations to control level of Diethylene glycol and Ethylene glycol • General Public |
| Problem or Issue: | World Health Organization (WHO) has issued Medical Product Alert No. N°6/2022 dated 05th October 2022 which refers to four substandard products, identified in Gambia. These four products are Promethazine Oral Solution, Kofexmalin Baby Cough Syrup, Makoff Baby Cough Syrup and Magrip N Cold Syrup. Laboratory analysis of samples of each of the four products confirm that they contain unacceptable amounts of diethylene glycol and ethylene glycol as contaminants. DRAP has never authorized sale of any products from Maiden Pharmaceuticals Limited (Haryana, India) and these four products referred in WHO medical product alert are neither registered nor available on Pakistan market, however these may have been carried for personal use while visiting other countries. Please do not use any of these products as these are substandard products and their use may result in serious injury. |
| Potential Hazards linked to DEG and EG: | Toxic effects can include abdominal pain, diarrhea, inability to pass urine, headache, altered mental state, vomiting and acute kidney injury which may lead to death especially in children |
| Advice for healthcare professionals: | DRAP requests increased vigilance within the supply chains of institutions/pharmacies/healthcare facilities to detect any substandard / falsified product in the market. Adverse reactions or quality problems experienced with the use of any product shall be reported to the National Pharmacovigilance Centre(NPC), DRAP using Adverse Event Reporting Form or online through this link. Further information of reporting problems to DRAP is available on this link. |
| Advice for Manufacturer’s and Importers of Products containing Glycerin Solvent: | Unacceptable amounts of Diethylene glycol (DEG) and Ethylene glycol (EG) as contaminants may lead to severe injury or death. You are therefore advised to strictly follow the pharmacopoeia guidelines for excipients and ensure testing of all those products where diethylene glycol and ethylene glycol can appear as impurity, to ensure specifications limits are being comply for all those products where glycerin is used especially cough syrups and other oral products. |
| Advice for General Public: | All therapeutic goods must be obtained from the licensed pharmacies, and other authorized retail outlets. The authenticity and condition of products should be carefully checked. Seek advice from your pharmacists or other healthcare professional in case of any doubt. |
| Guidelines for reporting Adverse Drug Reactions (ADRs): | Both healthcare professionals and patients are requested to report any adverse events they have experienced to the National Pharmacovigilance Centre, Drug Regulatory Authority of Pakistan through DRAP Med Vigilance E-reporting system or at npc∂dra.gov.pk. Similarly, adverse events can also be reported through Med Safety Mobile Application that is available for download from the App store (For iOS devices) and Google Play (For Android devices). |
| References: | Medical Product Alert No. N°6/2022 |
Recall Alert: Drug Product; Human Albumin 20% 100mL (Batch/Lot # C236821P02) Manufactured By M/s. Biotest Pharma GmbH
Recall Alert
| DRAP Alert No | NoI/S/10-22-25 |
| Action Date | 7th October 2022 |
| Target Audience | 1. Pharmacists and Chemists at Distribution, Pharmacies and Medical Stores 2. Healthcare Professionals- Physicians, Pharmacists, and Nurses at hospitals, Clinics and Healthcare Providing Institutions 3. General Public |
| Product(s) Affected | Human Albumin 20% 100mL (Biotest), Active Ingredient(s): Serum Albumin 20% (Human) Company: M/s. Biotest Pharma GmbH, Germany imported by M/s Eastren Trade & Distribution Co, (Pvt) Limited, Karachi Batch No. C236831P02 Manufacturing Date: 17-Sep-2021, Expiry Date: 31-Aug-2024 |
| Problem Statement | DRAP has received a rapid alert from the Paul-Ehrlich Institut, Federal Institue of Vaccine and Biomedicines, Ministry of Health, Germany, with respect to the quality defect and voluntary recall of 06 batches of Human Albumin 20%, 100mL manufactured by the Botest AG, GmbH. Out of these six batches, one batch was imported in Pakistan by the authorized registration holder M/s Eastren Trade & Distribution Co, (Pvt) Limited, Karachi. |
| Action Initiated | The importer has been directed to immediately recall the stock of defective batch C236831P02 from the market. Regulatory field force is directed to supervise the recall progress. -All Pharmacists and chemists working at distributions and Pharmacies are required to immediately return the stock of above-mentioned batch of product to the supplier / importer / company. -Distributors and pharmacies are advised to be vigilant and report any suspected batch of product(s) in the supply chain to the DRAP using online form, or through phone at +92 51 910 73 17, or Email at gsms∂dra.gov.pk. -Regulatory field force of all federating units (DRAP, Provincial Health Departments and States) has also increased the surveillance in the market to ensure the effective recall of defective product(s). |
| Advice for Healthcare Professionals | -DRAP requests increase vigilance within the supply chains of healthcare institutions and hospital pharmacies to identify and return the defective batch(es) of this product to the importer / company. -Adverse reactions or quality problems experienced with the use of this product may be reported to the National Pharmacovigilance Centre(NPC), DRAP using Adverse Event Reporting Form or online through this link. -Please click here for further information on problem reporting to DRAP. |
| Advice for Consumers | -Consumers should stop using this product bearing the affected batch number(s) and shall contact to their physician or healthcare provider(s) if they have had experienced any problem that may be related to taking or using this product. -All drug products must be obtained from the authorized licensed pharmacies /outlets. Their authenticity and condition should be carefully checked. If you have any doubt, please seek advice from your pharmacist. |
Recall Alert: Drug Product; Fentos 50mg Tablets (Batch # 599) By M/s. Hisun Pharmaceutical Industries, Gadoon-Pakistan
Recall Alert
| DRAP Alert No | NoII/S/09-22-21 |
| Action Date | 6th October, 2022 |
| Target Audience | 1. Pharmacists and Chemists at Distribution, Pharmacies and Medical Stores 2. Healthcare Professionals- Physicians, Pharmacists, and Nurses at hospitals, Clinics and Healthcare Providing Institutions 3. General Public |
| Product(s) Affected | Fentos 50mg Tablets, Active Ingredient(s): Diclofenac Potassium Company: M/s. Hisum Pharmaceutical Insutries Gadoon, Pakistan Batch No. 599 Manufacturing Date: Sep-2021, Expiry Date: Sep-2023 |
| Problem Statement | The Central Drug Laboratory Karachi has analyzed the sample of Fentos 50mg Tablets (Registration No. 047810) bearing Batch No. 599, and declared it as Substandard. The company has been directed to recall the affected batch of product from the market. |
| Action to be taken | -All Pharmacists and chemists working at distributions and Pharmacies are required to immediately return the stock of above mentioned batch of product to the company. -Distributors and pharmacies are advised to be vigilant and report any suspected batch of product(s) in the supply chain to the DRAP using online form, or through phone at +92 51 910 73 17, or Email at gsms∂dra.gov.pk. -Regulatory field force of all federating units (DRAP, Provincial Health Departments and States) have also increased surveillance in the market to ensure the effective recall of defective product(s). |
| Advice for Healthcare Professionals | -DRAP requests increased vigilance within the supply chains of healthcare institutions and hospital pharmacies. -Adverse reactions or quality problems experienced with the use of this product may be reported to the National Pharmacovigilance Centre(NPC), DRAP using Adverse Event Reporting Form or online through this link. -Please click here for further information on problem reporting to DRAP. |
| Advice for Consumers | -Consumers should stop using this product bearing the affected batch number(s) and shall contact to their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. All drug products must be obtained from authorized licensed sources/outlets. Their authenticity and condition should be carefully checked. Seek advice from a healthcare professional in case of any doubt. |
Recall Alert; Drug Product: Pantoloon 20mg Tablets (Batch # 5611) By M/S. Rock Pharmaceutical Laboratories (Pvt.) Ltd. Risalpur
Recall Alert
| DRAP Alert No | NoII/S/09-22-22 |
| Action Date | 5th October, 2022 |
| Target Audience | 1. Pharmacists and Chemists at Distribution, Pharmacies and Medical Stores 2. Healthcare Professionals- Physicians, Pharmacists, and Nurses at hospitals, Clinics and Healthcare Providing Institutions 3. General Public |
| Product(s) Affected | Pantoloon 20mg Tablets, Active Ingredient(s): Pantoprazole Company: M/s. Rock Pharmaceutical Laboratories (Pvt.) Ltd. Risalpur . Batch No. 5611 Manufacturing Date: May-2022, Expiry Date: Mar-2024 |
| Problem Statement | The Central Drug Laboratory Karachi has analyzed the sample of Pantoloon 20mg Tablets (Registration No. 095091) bearing Batch No. 5611, and declared it as Substandard. The company has been directed to recall the affected batch of product from the market. |
| Action to be taken | -All Pharmacists and chemists working at distributions and Pharmacies are required to immediately return the stock of above mentioned batch of product to the company. -Distributors and pharmacies are advised to be vigilant and report any suspected batch of product(s) in the supply chain to the DRAP using online form, or through phone at +92 51 910 73 17, or Email at gsms∂dra.gov.pk. -Regulatory field force of all federating units (DRAP, Provincial Health Departments and States) have also increased surveillance in the market to ensure the effective recall of defective product(s). |
| Advice for Healthcare Professionals | -DRAP requests increased vigilance within the supply chains of healthcare institutions and hospital pharmacies. -Adverse reactions or quality problems experienced with the use of this product may be reported to the National Pharmacovigilance Centre(NPC), DRAP using Adverse Event Reporting Form or online through this link. -Please click here for further information on problem reporting to DRAP. |
| Advice for Consumers | -Consumers should stop using this product bearing the affected batch number(s) and shall contact to their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. All drug products must be obtained from authorized licensed sources/outlets. Their authenticity and condition should be carefully checked. Seek advice from a healthcare professional in case of any doubt. |
Recall Alert; Drug Product: Zatranex 50mg/mL injection (Batch # 622) by M/s. Zafa Pharmaceutical Laboratories (Pvt.) Ltd., Karachi.
Recall Alert
| DRAP Alert No | NoI/S/09-22-23 |
| Action Date | 5th October, 2022 |
| Target Audience | 1. Pharmacists and Chemists at Distribution, Pharmacies and Medical Stores 2. Healthcare Professionals- Physicians, Pharmacists, and Nurses at hospitals, Clinics and Healthcare Providing Institutions 3. General Public |
| Product(s) Affected | Zatranex 50mg/mL Injection, Active Ingredient(s): Tranexamic Acid Company: M/s. Zafa Pharmaceutical Laboratories (Pvt.) Ltd., Karachi. Batch No. 622 Manufacturing Date: April-2022, Expiry Date: April-2025 |
| Problem Statement | The Central Drug Laboratory Karachi has analyzed the sample of Zatranex 50mg/ml Injection (Registration No. 014217) bearing Batch No. 622, and declared it as Substandard. The company has been directed to recall the affected batch of product from the market. |
| Action to be taken | -All Pharmacists and chemists working at distributions and Pharmacies are required to immediately return the stock of above mentioned batch of product to the company. -Distributors and pharmacies are advised to be vigilant and report any suspected batch of product(s) in the supply chain to the DRAP using online form, or through phone at +92 51 910 73 17, or Email at gsms∂dra.gov.pk. -Regulatory field force of all federating units (DRAP, Provincial Health Departments and States) have also increased surveillance in the market to ensure the effective recall of defective product(s). |
| Advice for Healthcare Professionals | -DRAP requests increased vigilance within the supply chains of healthcare institutions and hospital pharmacies. -Adverse reactions or quality problems experienced with the use of this product may be reported to the National Pharmacovigilance Centre(NPC), DRAP using Adverse Event Reporting Form or online through this link. -Please click here for further information on problem reporting to DRAP. |
| Advice for Consumers | -Consumers should stop using this product bearing the affected batch number(s) and shall contact to their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. All drug products must be obtained from authorized licensed sources/outlets. Their authenticity and condition should be carefully checked. Seek advice from a healthcare professional in case of any doubt. |