Technical Information for Life-Saving Mnch Products

Technical Information for Life-Saving Mnch Products

Module II | Programic Approach to Assure Quality of MNCH Products MODULE III TECHNICAL INFORMATION FOR LIFE-SAVING MNCH PRODUCTS OXYTOCIN MISOPROSTOL MAGNESIUM SULFATE GENTAMICIN 7.1% CHLORHEXIDINE DIGLUCONATE AMOXICILLIN ORAL REHYDRATION ZINC MIIꟷ1 MODULE III TECHNICAL INFORMATION FOR LIFESAVING MNCH PRODUCTS his module provides useful technical information on the UNCoLSC’s life- saving MNCH products to assist the procurement agencies in establishing T technical specifications for the product(s) to be prequalified and/or evaluating the product information package submitted by the manufacturer when full assessment is necessary. The information provided in this module is based on review of compendial monographs and literature, and on internal expert consultations. The following UNCoLSC’s life-saving MNCH products are included in this module . Maternal health Newborn Child health Oxytocin Gentamicin Amoxicillin Injection 10 IU in 1-mL Injection Dispersible tablets, 250 mg 10 mg/mL in 2 mL vial Misoprostol 40 mg/mL in 2 mL vial Oral rehydration Tablets, 200 micrograms Solution 7.1% chlorhexidine Magnesium sulfate digluconate Zinc Injection Solution or gel Sulfate, gluconate, acetate, 500 mg/mL in 2-mL and citrate; dispersible tablets 10-mL ampoule 10 mg, 20 mg; oral solution 10 mg per unit dosage MIIIꟷ1 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities OXYTOCIN INJECTION 10 IU IN 1-ML GENERAL PRODUCT INFORMATION Postpartum hemorrhage (PPH) refers to excessive bleeding after childbirth. Left untreated, it can lead to anemia, shock, and also death. PPH is the leading cause of maternal death in low- and middle-income countries. Proper screening, prevention, and treatment of PPH can save women’s lives and reduce global burden of maternal mortality. Prevention and treatment for most cases of PPH require the use of an uterotonic medicine to increase muscle contractions in the uterus that compress the blood vessels. Oxytocin is recommended by WHO as the first-line medicine for the prevention and treatment of postpartum hemorrhage. It is also prioritized as an essential medicine by the UN Commission on Life-Saving Commodities for Women and Children. Other uterotonic medicines, such as misoprostol, ergotamine and ergometrine, have some drawbacks. Misoprostol is the second-line medicine, recommended by the WHO for the prevention and treatment of PPH only when oxytocin use is not feasible. It is recommended for use in women giving birth outside of a health facility (e.g., home deliveries), as it is administered by pill rather than by injection. Ergotamine and ergometrine have more side effects, should only be given after the birth of the placenta, must be kept in the cold chain, and are contraindicated for many conditions, including pre-eclampsia. Oxytocin is the safest and most effective uterotonic medicine for the prevention and treatment of PPH, which should be procured over other uterotonic medicines and made available in all health facilities to help lower maternal death rates and improve overall maternal health. Oꟷ1 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities Oxytocin KEY CONSIDERATIONS IN PROCUREMENT Procurement should be made from trusted sources. This includes manufacturers prequalified by WHO, approved by an SRA, or recommended 1. by the ERP and with a proven record of quality products. Procurers need to focus on product quality to ensure the product is sterile and 2. safe for patient use as oxytocin is an injectable medicine. KEY QUALITY CONSIDERATIONS Product specification Oxytocin injection products must comply with the quality specifications as detailed in “Product Specifications” section below. Packaging and labeling The container-closure system (ampoule/vial) must be sufficient to preserve sterility during the shelf life of the product. Additional information about oxytocin injection packaging and labeling can be found in Annex A2 item 4. Storage, transportation, and distribution Oxytocin that is procured should be labeled and stored between 2˚C and 8˚C from the point of manufacture to the point of use to maintain the product quality. Although some manufacturers state the product can be stored at controlled room temperature, between 20˚C and 25˚C, it should be noted that room temperatures in health facilities in tropical countries often exceed the controlled room temperature, which can put oxytocin quality at risk. Oxytocin is temperature-sensitive and loses effectiveness after three months of storage at temperatures above 30˚C. Significant quality issues can stem from inappropriate transport and storage, which may expose the product to high temperatures that can degrade it and result in low potency. Detailed records of all stages of transport from the date the oxytocin product leaves the FPP manufacturer to its arrival at the procurer facility should be provided to assure the product has not been subject to adverse temperatures for a potentially harmful length of time. The procurer should reach agreement with the FPP manufacturer and/or distributor to use the most suitable transport and handling to protect the product from exposure to high temperatures. Data loggers or suitable temperature-time integrators can be used to alert procurers of any excursions during transportation and be alert to possible degradation of oxytocin. Oꟷ2 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities Oxytocin Name of the Oxytocin injection Medicinal Product Chemical Oxytocin (L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutamyl-L-asparaginyl-L- Name cysteinyl-L-prolyl-L-leucylglycinamide cyclic (1→6)-disulfide) Oxytocin is a synthetic cyclic nonapeptide having the structure of the hormone produced by the posterior lobe of the pituitary gland that stimulates contraction of the uterus and milk ejection in receptive mammals. Being wholly synthetic, it does not contain vasopressin and has a constant and reliable effect. Chemical C43H66N12O12S2 Structure Pharmaceutical Sterile solution for injection Form A clear, colourless solution Qualitative and Oxytocin injection is a sterile solution of oxytocin or a sterile dilution of Quantitative oxytocin concentrated solution in water for injection. It contains 10 IU of Composition oxytocin per mL. List of possible excipients1: – Acetic acid – Chlorobutanol – Ethanol – Sodium acetate trihydrate – Water for injection Packaging and The WHO Essential Medicines List states “oxytocin injection 10 IU in 1- Presentation mL,” which does not preclude procurement of any particular presentation of injectable oxytocin. Oxytocin injection is generally packed in glass ampoules. However, some manufacturers provide the product in glass or plastic vial. 1 Based on the formulation of an innovator product, Syntocinon. Oꟷ3 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities Oxytocin SUPPLY Generally, products prequalified by the WHO PQP and/or approved by an SRA are considered quality-assured and highly recommended for procurement. In the absence of WHO-prequalified, SRA-approved, or ERP-recommended products, medicines from trusted sources, such as manufacturers approved by UN agencies, can be considered for procurement. Alternatively, the procurement agency may conduct its own quality assessment, as described in Module II. WHO-prequalified products As of February 2018, two oxytocin injections are prequalified by the WHO PQP, as shown below. It is recommended to check the updated information at the time of procurement, by going to https://extranet.who.int/prequal/content/prequalified-lists/medicines. Table O-1. List of WHO Prequalified Oxytocin Injection WHO REF. NUMBER RH050 RH053(a) MARKETING PT Sanbe Farma, Jl. Taman Sari no. 10, Grindeks JSC, 53 Krustpils AUTHORIZATION Bandung, 40116, Indonesia Street, Riga, 1057, Latvia HOLDER MANUFACTURING FPP manuf. site: PT Sanbe Farma, Sterile FPP manuf. site: HBM Pharma SITE Preparation Plant, Unit 3, Jl. Industri SRO, Sklabinska 30, Martin, 036 Cimarene No. 8, Desa Cimareme, 80, Slovakia Kecamatan Ngamprah, Kabupaten Bandung Barat, 40553, Indonesia API manuf. site: Grindeks JSC, 53 API manuf. site: Grindeks JSC, Krustpils Street, Riga, 1057, Latvia 53 Krustpils Street, Riga, 1057, Latvia DOSAGE FORM Solution for injection 10 IU/mL Solution for injection 10 IU/mL AND STRENGTH PACKAGING AND Ampoule; Type I glass Ampoule; Type I glass PRESENTATION 1 mL x 10’s 1 mL x 5’s 1 mL x 10’s DATE OF PRE- June 30, 2017 April 16, 2015 QUALIFICATION SHELF LIFE 18 months 48 months STORAGE Store in refrigerator (2–8˚C), Store in refrigerator (2–8˚C), CONDITION do not freeze, protect from light. protect from light. (a) Indicates SRA-approved product that has been prequalified based on abbreviated assessment. Oꟷ4 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities Table Oxytocin O MARKETING ꟷ AUTHORIZATION REGISTRATION PACKAGING AND SHELF 5 PRODUCT NAME SRA HOLDER NUMBER PRESENTATION LIFE STORAGE CONDTION | O Manual for Procurement & Supply of Quality of Supply & Procurement for Manual ® - Syntocinon 10 UK Novartis PL 00101/0960 Clear glass 1-mL 5 years Store in refrigerator (2–8˚C). May be 2. IU/mL concentrate MHRA Pharmaceuticals UK ampoule stored up to 30˚C for 3 months, but Examples o for solution for Ltd, UK must then be discarded. infusion Oxytocin 10 IU/mL UK Peckforton PL 15760/0036 Transparent Ph. 4 years Store in refrigerator (2–8˚C). May be f S solution for infusion MHRA Pharmaceuticals Ltd, Eur. type I glass 1- stored up to 30°C for 3 months but RA UK mL ampoule must then be discarded. - Approved

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