The Food and Drugs Authority (FDA) has said the deaths of three persons at the New Senchi Health Centre at Akrade in the Eastern Region from some injections may have been caused by contaminated medication.
The medication in question, o.9% Normal Saline, is believed to have been contaminated after being used multiple times, according to a statement from the FDA.
[contextly_sidebar id=”HwoIKeXY2LeKr7ke8tlOngIzQ8IFVful”]The deceased include a 31-year-old man, a 42-year-old woman and a 78-year-old man.
The deceased persons suffered “adverse reactions described as injection site abscess, skin necrosis and ulcers leading to the deaths,” the FDA said.
“Preliminary investigations revealed that these reactions may be due to contaminated 0.9% Normal Saline, the solution which was used to reconstitute (mix) the Benzathine Penicillin Powder for Injection. The 0.9% Normal Saline Solution was reported to have been opened and used repeatedly for several days which might have resulted in the contamination,” the statement from the FDA explained.
The FDA has also dispatched a team to Akrade to investigate the issue in collaboration with the Ghana Health Service.
The Director of Public Health at Ghana Health Service, Dr. Badu Sarkodie earlier confirmed the developments to Citi News and said the service was in the process of compiling a situational report.
Find below the full FDA statement
SERIOUS ADVERSE REACTION REPORTS, NEW SENCHI HEALTH CENTRE, AKRADE
The Food and Drugs Authority (FDA) has become aware of serious adverse reactions described as injection site abscess, skin necrosis and ulcers leading to the deaths of three (3) patients who had injections of Benzathine Penicillin from the New Senchi Health Centre at Akrade in the Asuogyaman District in the Eastern region. These serious adverse reactions were reported during the 3rd week of March 2018.
Preliminary investigations revealed that these reactions may be due to contaminated 0.9% Normal Saline, the solution which was used to reconstitute (mix) the Benzathine Penicillin Powder for Injection. The 0.9% Normal Saline Solution was reported to have been opened and used repeatedly for several days which might have resulted in the contamination.
Benzathine Penicillin is presented as powder for Injection and should be reconstituted with STERILE water for injection and also used immediately to avoid contamination.
The FDA has dispatched the Pharmacovigilance team from the Eastern Regional Office to Akradie to investigate the issue in collaboration with the Ghana Health Service and will keep you updated as more information becomes available.
Meanwhile, healthcare professionals and consumers are encouraged to be vigilant and report untoward effects of medicines and health products to the FDA by completing adverse reaction reporting forms provided in hospitals and Community Pharmacies designated as Patient Safety Centres across the country or through the contacts below:
HOTLINES – 0299802932, 0299802933,
TOLL FREE NUMBER – 0800151000 (free only on Airtel and Vodafone)
SMS SHORTCODE – 4015
SIGNED
CHIEF EXECUTIVE OFFICER
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By: Delali Adogla-Bessa/citifmonline.com/Ghana