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Cabinet of Ministers Regulations No. 435 in Riga in 2007 (26 June. No 37 34) amendments to the Cabinet of Ministers of 8 March 2005, regulations No 175 "prescription form manufacturing and storage, as well as prescription" Issued in accordance with article 60 of the law on medical treatment and the law "on the illicit manufacture of narcotic drugs and psychotropic substances and to the legitimate movement of medicinal products order" 36. the first paragraph of article 1 do cabinet 8 March 2005 rules no 175 "prescription form manufacturing and storage, as well as the rules of prescription" (Latvian journal 48., 2005, no.) the following amendments: 1. provisions of title be expressed by the following: "prescription form manufacturing and storage, as well as prescription and storage"; 1.2. the express indication on what basis the provisions of the law, issued by the following: "Issued in accordance with article 60 of the law on medical treatment and the law" on the illicit manufacture of narcotic drugs and psychotropic substances and to the legitimate movement of medicinal products order "article 36 the first part"; 1.3. make 5, second sentence by the following: "prescription form is printed on white paper with watermarks."; 1.4. to make the first sentence of paragraph 6 in the following wording: "the usual recipes form borders and fills in part of the pharmacy, is highlighted in light blue."; 1.5. make the following paragraph 11: "11." special prescription form and medical institution within the Agency recorded special prescription form log in to be able to provide prescription form and movement control. Special prescription form log sample shall be determined respectively by the Director of the Agency and the hospital's Manager. "; 1.6. to replace paragraph 16, first sentence, the words "which is placed against the unauthorised access to and provided with an alarm-equipped room" with the words "which is placed against the unauthorised access to the site"; 1.7. to express 17 as follows: "17. Scrap, broken, removed from the market in prescription form and unused prescription record invalid prescriptions and prescription form log in to ensure the prescription form and movement control, including by making a mark on the prescription form or prescription and withdrawn from circulation prescription form transfer agency (number and date of the Act). Not valid prescription form and prescription log sample shall be determined respectively by the Director of the Agency and the hospital's Manager. "; 1.8. to make 21 the following: "21. If it finds the special prescription form discrepancies or surplus, have been theft, robbery or loss due to natural disasters, the deposit box sealed and the underlying fact is immediately reported to the medical care and integrity inspection quality control inspection, as well as the national police (if there has been a theft or robbery). "; 1. replace paragraph 24, first sentence, the words "(at least three person)" with the words "(at least two person)"; 1.10. the express 27 the following: 27.35. These rules repeatedly referred to all the recipes use prescribed medicine for the quantity stored in the patient, but the pharmacy, not the drug, prescription signed copies of both sides and keep a copy of these rules in paragraph 26, the usual prescription for the storage time. After all, in the volume of prescriptions issued prescription pharmacy, retaining the last purchase. "; 1.11. Express 34 as follows: "34. Medication containing buprenorphine may be invoiced only for the patient, which narkolog State limited liability company" Riga psychiatric and addiction centre "has been issued by a buprenorphine substitution therapy programs. Narkolog news on the name of prescriptions, the dosage, quantity, date and number of the recipes also indicate that the map program. The acquisition of the medicinal products in the recipes that contain buprenorphine, patient statement more frequently than every two weeks. " 1.12. supplement with 34.1, 34.2 and 21.3 points as follows: 34.1 "drugs, which, in accordance with the regulations on the procedure for the classification of the medicinal product is intended for outpatient treatment, but can cause serious side effects, which are necessary for use in the treatment of industry guidance and supervision throughout the treatment period, and which is applied to the term" Pr "on medical specialty II indication may be invoiced only specified specialty doctor. 21.3 prescribing medications, the use of which may lead to increased health risks and the use of which should be particularly monitored, observe the registration certificate holder (owner) and developed with the State Agency of medicines of the agreed use of the medicinal product concerned risk prevention programs. Registration certificate holder (owner) this program provides access to doctors who have the right to prescribe the medicinal product concerned. 21.3 medicinal products containing isotretinoin, reproductive age women may make no more than one month long treatment course, given in accordance with the provisions set out in article 34.2 of the registration certificate holder (owner) and developed with the State Agency of medicines of the harmonized programme planning pregnancy. Registration certificate holder (owner) provides pregnancy planning programs availability of doctors, who have the right to prescribe medications containing isotretinoin. "; 1.13. Express 39 the following: "39. Prescribing a prescription psychotropic drug (excluding this provision referred to in paragraph 38 cases) and the Narcotic analgesics for the acquisition of the funds, the doctor orders a medication course for up to one month. Narkolog, psychiatrist, neurologist and family physician compensation procedures within the framework of such products can make a treatment course for up to three months. " 1.14. the express 48 as follows: "48. specific recipes the validity is 30 days. The usual prescription is expired three months apart: 29.9. prescription, charged this provision referred to in paragraph 3 and the validity of which is seven days; 48.2. This provision, paragraph 36, repeatedly used in the recipe, which validity period (not exceeding one year) the doctor determined. "; 1.15. Express 30.8. subparagraph by the following: "30.8. physician's name, surname, personal code and specialty;"; 1.16. the deletion of the words in subparagraph 49.7. "(if the recipes extract medicinal product or medical device according to the prescribed refund procedure)"; 1.17. supplement 49.10. subparagraph after the word "name" with the words "and code"; 1.18. the express section follows 49.11.: 49.11. for medicinal products granted code and quantity (number of packages). Compensation procedures within distributed drugs in addition to specify one package price, pay the amount (taking into account the number of packages) and its distribution between the patient and other persons; " 1.19. supplement with 55.1 and 55.2 point as follows: "55.1 is permitted by the national agency of medicinal products designed electronic recipes use the typographic printed recipes to complete parallel functioning of electronic prescription system. Electronic prescription contents meeting the requirements of this regulation, and is in accordance with the legislation on electronic documents. 55.2 medicine and medical position devices on prescription forms, printed up to 2007 and 30 September, allowed until May 1, 2008. "; 1.20. Express annex 1 as follows: "annex 1: Cabinet of Ministers of 8 March 2005, regulations No 175 regular recipes model form" 1.21. make annex 2 as follows: "2. the annex to Cabinet of Ministers of 8 March 2005, regulations No 175 recipes Special model form" annex 3 deleted 1.22 (1); 1.23. Express 3. point 2 of the annex by the following: "2. in the introductory part of the recipe (Inscripti): 2.1 recipes date; 2.2. the name, surname, personal code (E-bearer form identification number) and address. The doctor when the conventional recipe for personal use, the patient's first and last name is a "Pro me" (my) or "ad" of CSR propriu (for personal use), but address the site indicates your actual home address, and phone number; 2.3. the hospital's name, number, address, and phone number; 2.4. the medical treatment person's first name, last name, specialty and personal code, which extract recipe. "; 1.24. the supplement to annex 3 paragraph 10, after the word "after" with the words "how often"; 1.25. the supplement to annex 3 paragraph 15, after the word "code" with the words "in accordance with international statistical problems of disease and health rankings (10) (further-classification of the SSK)"; 1.26. the supplement to annex 3 paragraph 17:1.26.1. drug follows the words "code" with the words "(registration number Latvia register of medicinal products)"; 1.26.2., after the word "name" with the words "(the name indicates, if the product is not included in the register of medicinal products)"; 1.27. Express 3. paragraph 20 of the annex by the following: "20. The insurance company's name and the amount of compensation, if the purchase of medicinal products reimbursable by insurance companies to the patient, pharmacist or the pharmacist indicated of an Assistant who shall issue, pursuant to the Hall with the insurance company contracts and insurance policies conditions."; 1.28. Express 3. 22. paragraph by the following: "22. any special recipes To the doctor indicates diagnosis code according to the classification of the SSK. When the Glycemic teststrēmel's pregnant women, in addition to the pamatdiagnoz code indicates code "Z33". "; 1.29. supplement to annex 3 22.1 points as follows: "a product to a particular Statement 22.1 recipes, the doctor tells the checkout code for medicinal products. Drug code: 22.1 1. reflect the drug code anatomic therapeutic chemical classification, if the product of the compensation statement, using the General name of the medicinal product; 22.1 2. medicinal products reflect the identification number of the eligible lists if the medicinal grass extract compensation procedures, except that rule 22.1 below. referred to in paragraph 1; 22.1 3. reflect the registration numbers Latvian register of medicinal products, if the product statement outside the compensation policy; 22.1.4 is specified, if the product is not included in the register of medicinal products. '; 1.30. the supplement to annex 3, paragraph 23, after the words "code" with the name of the medicinal product "(drug identification number in the list of medicinal products eligible compensation procedures izplatāmaj within the medicinal products or registration number in the register of medicinal products-Latvia in the other cases) or the title (the name indicates, if the product is not included in the register of medicinal products)"; 1.31. the supplement to annex 5, paragraph 5.1 by the following: "5.1 Hidromorfon hydrochloride 6.4" 2. Regulations shall enter into force by 1 October 2007.
Prime Minister a. Halloween Health-Welfare Minister d. Staķ, Minister of
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