Skip to main content

South Africans need to return 318,000 packets of potentially dangerous pills


The South African distributor of heart pills that may contain a potentially carcinogenic ingredient has confirmed that more than 318,000 packets of pills may be affected.
“Operationally, it is a difficult situation,” a representative of Pharma Dynamics, the distributor of the tablets in South Africa, told Business Insider South Africa.
The South African Health Products Regulatory Authority (SAHPRA) this week recalled Dynaval Co high blood pressure and heart pills, which may contain a controversial carcinogenic ingredient that was manufactured in China.
Dynaval Co 80/12.5 mg, 160/12.5 mg and 160/25 mg pills, which were manufactured by Zhejiang Huahai Pharmaceuticals, may contain the chemical NDMA.
NDMA is associated with liver damage and liver cancer in rats as part of laboratory tests, says dr Eric Decloedt, a clinical pharmacologist at the department of medicine of the University of Stellenbosch. “We extrapolate that it could hold the same risks for people.”
The affected pills contain the ingredient valsartan, but only tablets manufactured by Zhejiang may contain the NDMA. Dynaval 80 mg and 160 mg tablets are not affected.
The Dynaval Co pills were not available in the state health sector, but were in wide use among private patients, who used it for high blood pressure,  heart failure and as part of treatment after a heart attack.
According to Nicole Jennings, corporate communications manager of Pharma Dynamics, more than 318,000 packets of the pills are still in circulation. Anyone with a packet of Dynaval Co should urgently return the medicine to their pharmacy.
European authorities first announced a recall of the batch of medicines that was manufactured by Zhejiang earlier this month. It took a full three weeks for the local authorities to order its withdrawal in South Africa. 
"The responsibility of managing this matter and communicating this information to the public is shared by both SAHPRA and the manufacturers," a SAHPRA spokesperson told Business insider.
“Once SAHPRA was informed by Pharma Dynamics about the affected products, appropriate actions were undertaken in consultation with the manufacturer, to warn healthcare professionals and the public about this potential risk.”
She said that to date, SAHPRA has not identified other valsartan containing products that are affected.
At this stage reports around the impurity possibly causing cancer has not been verified by any health authority, said Jennings.  
“No definitive information has been received to indicate an immediate threat to patients as investigations are still underway."
People who have been using the medicine can get a refund from their pharmacies.
A Pharma Dynamics spokesperson warned that it is dangerous to just stop using the medication – they need to speak to a pharmacist or doctor first about a substitution. The company doesn’t have any immediate plans to foot these doctors’ bills, however.
Decloedt says other medicines containing losartan, candesartan or telmisartan – and pills that contain valsartan but not NDMA – could be prescribed.
please refer to our website for pharma regulatory documentation

Comments

Most Popular

Certificates of Analysis (CoA) World’s future of business is in outsourcing and globalisation EU GMP Guide Part I (Chapter 4 and Chapter 6) - these chapters contains detailed information about safety and quality, Laboratory documentation should follow the principles given in Chapter 4. EU GMP Guide Part II - Section 11.4 – §         Authentic Certificates of Analysis should be issued for each batch of intermediate or API on request. §         Information on the name of the intermediate or API including where appropriate its grade, the batch number, and the date of release should be provided on the Certificate of Analysis. For intermediates or APIs with an expiry date, the expiry date should be provided on the label and Certificate of Analysis. For intermediates or APIs with a retest date, the retest date should be indicated on the label and/or Certificate of Analysis. §  ...

What is Regulatory Intelligence (RI)?

If we will search for  RI  anywhere we will be getting many results and definitions. The act of gathering and analysing publicly available regulatory information. This includes communicating the Implications of that information, and monitoring the current regulatory environment for opportunities to shape future  regulations , guidance, policy and legislation. Regulatory Information collectively comprises of three main segments which are followed while performing Regulatory Information activities: •  Gather Data : RI professionals perform research about regulatory norms as per a particular product in a particular geography. As far as collecting relevant regulatory information is concerned, there are a lot of sources that RI professionals leverage to consolidate their research material. •  Analyse Information : This gathered data needs to be filtered out to obtain relevant information as per the purpose. The data filtered is then rearran...