Read the untranslated law here: https://www.vestnesis.lv/ta/id/104228
Cabinet of Ministers Regulations No. 175 in Riga, 8 March 2005 (pr. No 13, § 32) prescription form of manufacture and storage, as well as the rules of prescription are 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 a i. General questions 1. determine the prescription (excluding veterinary prescription) the manufacture and storage of forms, as well as the prescription order.
2.Ir the following prescription forms: 2.1 recipes form on which a statement of full payment to be served Hall and medical devices, except for the drug, psychotropic drugs and medicines which the State Agency of medicines is recognised by means of analgesics on drugs (hereinafter referred to as the usual recipes form) (annex 1);
2.2. a prescription form that extract the narcotic drugs and psychotropic drugs, including drugs, which the State Agency of medicines have been found by the Narcotic analgesics for features, as well as medicines and medical devices, the purchase of which the patient partially or completely offset the Castle (hereinafter special recipes form) (annex 2).
3. Advertising on recipes (recipes form the other side) is prohibited.
II. the prescription form and storage 4. Prescription forms shall be printed in accordance with the commercial rules 1 and 2 in the annex. The commercial printed recipes series and sequence numbers, noting that prescription form in the series, as well as a number of non-repeating series.
5. Recipes form size is 12 × 18 cm. Prescription form is printed on paper with a watermark. Iespiedtekst is black in color.
6. The usual recipes form borders and fills in part of the pharmacy is greyed indigo blue color. Special recipes form consists of two carbonless copies of forms: 6.1 a master form borders and fills in part of the pharmacy, are colored pale pink;
copies of the form UR6.2.otr like borders and fills in part of the pharmacy, is highlighted in yellow.
7. the prescription form and medical treatment to persons disseminating health compulsory insurance State Agency (hereinafter the Agency). The Agency shall, in accordance with the legislation on public procurement organized order prescription form, as well as for the manufacture of a prescription form of commercial printing, 5 and 6 of these regulations, paragraph defensive incorporated to prevent the prescription form of counterfeiting.
8. The merchant who, in accordance with the agency agreement entered into on commercial printed forms, provides prescription prescription prescription form and the form of the original photos used for the manufacture of storage so that they do not access by unauthorised persons. In the depressed commercial prescription forms together with the invoice, as well as of prescription forms used for the manufacture of the original photos from the Merchant shall provide to the Agency. The prescription forms scrap merchant passes the Agency drawing up the certificate.
9. The Director of the Agency shall designate officials responsible (designated officer): 9.1 prescription form from the merchant, who printed the form, the prescription records, storage and dispensing of medical institutions and medical treatment;
9.2. the prescription form of the photos used for the manufacture of the original receipt and storage, taking into account that the conventional prescription forms used for the manufacture of the original photos are stored in a single year, but special prescription form used for the manufacture of the original photos, three years;
UR9.3.br āķēt and withdrawn from circulation prescription form and destruction.
10. Treatment Services Manager and is responsible for the form, the prescription and dispensing of medical people who worked in the medical institution, as well as the unused special prescription records storage and destruction, which in accordance with the provisions of paragraph 25 of received from the patients (hereinafter explosive recipe), and withdrawn from circulation prescription form and transfer the records to the Agency, draw up the certificate.
11. Special prescription form and medical institution within the Agency recorded special prescription form log. The log indicates the following: 11.1. prescription form receipt date;
11.2.no as of prescription forms received (the Agency notes that the commercial operators holding his prescription forms, but the medical establishment shall provide to the agency or agencies);
UR11.3.sa number of the prescription form;
UR11.4.sa take the prescription form of the series;
UR11.5.sa the prescription form number (indicating from which number up to which included);
11.6. the prescription form date of issue;
7.3. prescription forms issued by (name and signature);
11.8. the prescription form;
7.4. the prescription form of the series;
11.10. the prescription form number (indicating from which number up to which included);
11.11. prescription form recipient (name, last name (if you receive treatment, including medical treatment institutions and forms of kum nosa request number), the recipient's signature);
11.12. prescription form balance.
12. the Agency special prescription form and the original kept in Leningrad region with an alarm-equipped vault that is placed against the unauthorised access to and provided with an alarm-equipped room. The usual prescription forms, and photos of them originals, as well as scrap and removed from the market in prescription form kept in a room that is secured against unauthorised access, noting that scrap and removed from circulation until the prescription form destruction kept separated to prevent mixing with valid prescription forms.
13. the responsible officer provides prescription forms issued by the head of the hospital's approved (the head of the hospital's signature and the hospital's seal). The request shall specify the hospital's properties, date, number, prescription number and type of form. The usual prescription forms issued after the doctor's written request. This request indicates the doctor's name, surname, qualification number, address, telephone number, prescription number of the form, date and confirm the information. Special prescription request form is valid for seven days. Special prescription form request agency holds three years, ordinary prescription request form — one year.
14. the responsible officer delivers to the conventional prescription request form to indicate the number of the prescription form, the prescription and the number series, the prescription form, date of issue and the issuer (name, surname). That information issuing and receiving pledges in the signature.
15. the Agency's prescription forms issued by the person who handled the hospital's head of mission with the hospital's mandate approved by the supervisor. Mandate indicates that officials are entitled to receive a special prescription form, the date of issue and number, as well as the validity period of not more than seven days. Officer, receiving a prescription form, submit a token and presented identity documents, and submit a letter of guarantee, if payment is made by wire transfer. The doctor, get a prescription drug from ordinary form for invoicing for personal use, produce an identity document, a diploma certifying his education, or a doctor's certificate.
16. Medical institution from the Agency received prescription forms, as well as of prescription withdrawn form circulation to their referral Agency and unused until the destruction of the recipes stored in a vault equipped with an alarm that is placed against the unauthorised access to and provided with an alarm-equipped room, noting that from the circulation of the prescription form and removed unused recipes stored in separated to prevent mixing with valid prescription forms. Treatment the person provides the prescription form received, to avoid access by unauthorised persons.
17. Scrap, broken, removed from the market in prescription form and unused prescription record invalid prescription prescription of form/log. The log indicates the following: 17.1. prescription form/prescription date of filing;
17.2. the prescription form/prescription form;
17.3. the prescription form/prescription;
17.4. the prescription form/prescription series;
17.5. the prescription form/prescription number (indicating from which number up to which included);
10.9. the prescription form/prescription applicant (name, surname, signature (if removed from the chain recorded the prescription form, the Agency shall indicate the name of the medical establishment, the certificate number and date));
17.7. the prescription form/prescription recipient (name, surname, signature);
UR17.8.atz those of the prescription form/prescription destruction (destruction of number and date. If removed from the chain recorded the prescription form, the medical institution shall indicate on the prescribed form transfer agency (number and date)).
18.11 and 17 of these regulations, paragraph log (log) page number and cauršuj. Log in to the authorities concerned the Manager before the first record made by the signature and stamp of authority.
19. records of registration number, and the journals they do not leave a free space and deleting entries. Fix the "Correct to believe", the responsible authorities or treatment Manager's signature and stamp of the Office concerned.
20. The medical authorities and the head of the Agency, set up by the Commission (including relevant institution employees) whose monthly checks, as the institution adhere to prescription order form storage, as well as of prescription forms inventory. The results of the inspection, the Commission shall draw up an inventory of the Act. Inventory statement of authority shall keep for a period of three years.
21. If the special prescription form shortage, surplus, there has been a theft, robbery or loss due to natural disasters, the wallet and the room sealed and secured against unauthorised access. 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).
22. paragraph 21 of these rules in the case of the head of the Authority set up by the Commission. The Commission is made up of: 22.1. the Manager or the authorized officer;
22.2. the responsible officer (if the incident happened in the Agency);
22.3. Medical care and integrity inspection quality control inspection.
23. The rules referred to in paragraph 22 of the Commission of the Act. The Act specifies the nature of the incident, the prescription form in the series, numbers, quantity, date of drawing up the Act and members of the Commission (the name and job title). Act shall be drawn up in triplicate and signed by all the members of the Commission. The first copy of the Act remains in the medical institution or Agency (if the incident happened in the Agency), the second pass and the availability of medical care inspection quality control inspection, and the third copy shall be sent within three days in the country's pharmaceutical authorities. If you have found a prescription form of shortfall (including theft or robbery), the State pharmaceutical inspectorate informs the pharmacy for the prescription form and numbers.
24. Scrap and removed from the circulation of the prescription form, the form and the corrupted prescription unused prescription medical institution destroyed respectively, the agency or the hospital's managers created a Commission (at least three person). On the prescription form/prescription shall be drawn up in an act of destruction in duplicate, indicating the form of destroyed prescription/prescription form, series, numbers, quantity, location, date of disposal, disposal, other destruction related conditions, as well as members of the Commission (name and title). Legislation signed by all the members of the Commission. The first copy of the Act in the agency or medical institution shall keep for a period of three years, but the second copy of the act within three days, send the medical care and integrity inspection quality control inspection.
25. Medical treatment person when the special recipe for the illicit manufacture of narcotic drugs or psychotropic medicines recognized purchase, inform the patient that unused special recipes to be medical institution in which they are discharged.
26. the special recipes, which is a prescription narcotic drugs or psycho recognized tropical medicine, pharmacy stores in five years, but the other special recipes stored in three years. The usual prescription pharmacy stores in one year.
27. This provision 35, paragraph reusable recipe to all prescribed medicine for the quantity stored in the patient. After all, in the volume of prescriptions issued prescription keep pharmacy.
28. If on special prescription medicines is discharged or medical devices, the purchase of which the patient partially or completely covered from the purchase of medicines compensation granted funds according to regulations for outpatient treatments of medicines and medical equipment purchase expense allowance (hereinafter referred to as the compensation procedures), the second copy of the prescription pharmacy pass agency according to the concluded contract for health services. If on special prescription prescribed medication acquisition expenses partially or fully covered by the insurance company, the second copy of the prescription pharmacy pass insurance company in accordance with the signed agreement of the medication. If on special prescription prescriptions of acquisition expenses, they are not intended to compensate for the second copy to the pharmacy after the conclusion of the transfer of the patient the prescription.
III. procedures for prescription prescription 29 to determine the look of the ga forms (annexes 1 and 2), subject to the rules referred to in annex 3 of the prescription form filling requirements. Prescription clearly legibly by hand or using a computer or other technical means, which provides clear and unambiguous data perception. Medical person to receive and store prohibited prescription forms, which indicates the name of the medicinal product.
30. the recipes and text properties are clearly legible and indelible. When the recipe is not acceptable errors and corrections. Two special recipes to be identical copies of the completed and approved.
31.Uz Recipes extract the drugs and medical devices patient primary and secondary outpatient treatment. To write out the recipes prohibited drugs and medical devices medical practice.
32. The right to prescribe the usual prescription is a physician and a physician's Assistant (feldšer), which works in a medical institution. A doctor who does not work in the medical institution, allowed to discharge grass onto the usual recipes only for personal use.
33. The right to prescribe special recipe is just a doctor who works in a medical institution. The right to prescribe the drugs and medical devices according to the prescribed order of compensation is a doctor who has a contractual relationship with the Agency.
34. the medicinal products containing buprenorphine may be invoiced only for the patient, which narkolog At the National Agency issued the 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.
35. If a doctor prescribing medication to the usual recipes form, provides for the possibility of the patient buy medicine on a regular basis, the volume of prescriptions to pharmacies receive the parts no more than once a month, a physician on the prescription indicates "course of treatment". This indication the doctor confirms with a signature and a personal stamp, and this recipe is considered reusable recipe.
36.Uz form one prescription drugs and medical devices statement of not more than three months long course of treatment, with the exception of those rules specified in annex 4 of the medicine that the doctor that provision referred to in paragraph 35, repeatedly used the recipe you can make a treatment course for up to one year.
37.Uz one special recipes form allowed to discharge only one drug or medical device, secondary packaging (packaging) provides for up to three months for a treatment course.
38. when the recipe to the illicit manufacture of narcotic drugs and psychotropic medicines recognized, the doctor does not exceed this rules set out in annex 5 in the illicit manufacture of narcotic drugs and psychotropic substances recognized as the maximum quantity authorised for issue on one of the recipes.
39. Prescribing prescription psychotropic medicine purchase, except for this provision, the case referred to in paragraph 38, the doctor will extract no more than one package. Narkolog, psychiatrist, psychotherapist, neurologists and family physicians, if necessary, may make such products a treatment course for up to one month to form indicating the prescription "course of treatment" and confirm by signature and personal stamp.
40. If the person is a patient of treatment of narcotic drugs or psychotropic extract medicines or drugs which the State Agency of medicines is recognised by means of analgesics on drugs, it shall record the patient in outpatient card and specifies the name of the medicinal product concerned, dose, quantity and date. Treatment services manager at least once a month to ensure that the therapeutic medicines correctness and accuracy checking.
41. Alcohol or alcohol water solution treatment a person on a normal prescription forms. The recipes up to 96% of the statement 150 g alcohol or alcohol water solution, or the pharmacy made products containing up to 150 g 96% alcohol.
42.Uz recipes drawn from such prohibited means of anaesthesia: UR42.1.GHB (sodium oksibutirāt and lithium oksibutirāt;)
26.2. fentanyl injection solution;
26.3. diethyl ether.
43. when the recipe only allowed to use this provision in annex 6 of the abbreviations used in Latin.
44. the conventional recipe for treatment of persons with signature and personal stamp. If the statement of the special recipe, in addition to the need for the hospital's seal (practitioner may use a personal stamp, which includes medical practice properties).
45. If the medical person pharmacy in the cases specified in the law, the statement of the recipe for the purchase of medicinal products, which are not included in the register of the Republic of Latvia in the list of medicinal products, it shall inform the patient about this drug purchasing procedures.
46. at the request of the medical treatment a patient person who issued the statement, a copy or a copy of the prescription. Pharmacy service to the prohibited drugs or medical devices to copy, the copy of the prescription or the second copy.
47. the treatment of persons prohibited to issue a patient not filled or partially filled prescription form, except that the provisions referred to in annex 3 cases when individual recipes properties may not be specified.
48. the period of validity of the special recipes is 30dien. The usual recipes the validity is three months, except for this provision, paragraph 35 reusable recipe, which validity period (not exceeding one year) down the doctor.
IV. The Pharmacy and the duties of the public authorities and the prescription form prescription movement 49. Where medicinal products and medical devices to specific prescriptions prescription forms, the pharmacy in accordance with a contract for data processing electronic prescription to provide the Agency with the following information: 30.5. recipes series and number;
30.6. the Eveidlap type (if the recipe is drawn for another Member State of the European Union, Norway, Iceland, Liechtenstein or Switzerland's citizen under international treaty providing for mutual settlements for the health care services);
30.6. recipes date;
49. the name, surname and personal code (form E bearer — identification number);
30.8. hospital's name;
30.8. physician's name, surname and personal code;
49.7. diagnosis code (if the recipes extract medicinal product or medical device according to the prescribed refund procedure);
49.8. According to the prescribed compensation procedures applicable to compensatory interest;
31.0. the insurance company from sa Kuma (if purchase of medicines the patient is compensated for by an insurance company);
49.10. name of prescriptions;
49.11. code for medicinal products granted, the quantity (number of packages), one package price, pay the amount (taking into account the number of packages) and its distribution between the patient and other persons;
49.12. date of issue of the medicinal product.
50. the Agency: 50.1. accumulate and process these rules referred to in paragraph 49 of the prescription data;
50.2. provides quarterly reports to the Ministry of health for drugs and medical devices that are discharged to a special prescription form;
50.3. the National Agency for medicines, drug prices, a government agency, the national pharmaceutical inspection and enforcement institutions to request information on the medicines and medical equipment, issued on special prescription form;
50.4. the medical care and integrity inspection quality control inspection and law enforcement authorities request provides information about specific prescription.
51. Medical care and integrity inspection quality control inspection controls the prescription form of the movement order agency and medical institutions.
52. national pharmaceutical inspection controls the prescription order of chain pharmacies.
V. concluding questions 53. Special prescription form and prescription forms, to which the excerpt about differentiated pay Hall, printed up to this date of entry into force of the provisions, permitted to use up to 15 June 2005.
54. Ordinary prescription forms, printed up to the date of entry into force of the provisions, permitted until 30 June 2005.
55. Be declared unenforceable for Min three Cabinet on 14 July 1998 regulations No. 250 "prescription form of manufacture and storage and prescription rules" (Latvian journal, 1998, 212./213.nr.; 2001; 2003, No 7, no. 167).
56. This provision, paragraph 49 and 50 shall enter into force on 1 July 2005.
Prime Minister a. Halloween Health Minister g. Smith Editorial Note: the entry into force of the provisions by 24 March 2005.
1. the annex to Cabinet of Ministers of 8 March 2005, regulations No 175 Health Minister g. Smith annex 2 of the Cabinet of Ministers of 8 March 2005, regulations No 175 Health Minister g. Smith annex 3 of the Cabinet of Ministers of 8 March 2005, regulations No 175 Prescription form filling requirements i. General requirements 1. Recipes for the upper-left corner indicates the treatment code, name, address, and phone number. The doctor, when the usual recipe, recipes for personal use in the upper left corner indicates your actual home address, and phone number.
2. in the introductory part of the recipe (Inscripti) writes: 2.1 recipes date, month and year;
2.2. the name, surname, personal code (Eveidlap bearer — identification number) and address. The doctor when the conventional recipe for personal use, patient data is a "Pro" for me (for me) or "USA" ad of propriu (for personal use);
2.3. the medical treatment person's first name, last name, specialty and ID of the person who orders a prescription;
2.4. recipes the kids necessarily indicate the child's age (years, months, a child up to the age of one month – day).
3. Recipes in a part of the address (Invocati) writes "Rp.:" (recipe: take).
4. the recipes section (Praescripti of the materiar of s. Designati) after "Rp.:" the article pharmaceutical form, name with a capital letter in Latin, preceded the pharmaceutical form stating the dose and dose rate.
5. After the individual recipes products produced with a complex composition: 5.1 medicinal substances each name on a separate line in the article, first article of narcotic drugs, psychotropic and other strict accounting subject matter, then the others heavy exposure to substances and other active substances;
5.2. If the medicinal substances name is long, it allowed to continue into the next row;
5.3. medicinal plant names first name written with a capital letter, even if it is not located at the beginning of the line, but parts of the notation in this case written in lower case;
5.4. If the drugs because of their organoleptic characteristics assigned corrective substances, its article after the active substances;
UR5.5.pal īgviel that medicine provides the necessary consistency, shape, and quantity, the recipe written by last.
6. Recipes right from the constituents of the medicinal product concerned, to the name of the article quantity, volume or operations of mass units: 6.1 hard or soft bodied herbal substances — in grams or fractions of a gram, writing it as unnamed figures;
6.2. liquids: ml, writing behind the number, the abbreviation "ml";
6.3. the quantity of alcohol extract, in grammes of alcohol solution specifying;
6.4. number of drops is denoted by Roman numerals, writing it by the drop of the abbreviation "GTT".
6.5. medicinal action of active units indicates the number of units of action, followed by the abbreviation "MS" of the article.
7. If two or more of the constituents of the medicinal product to be equal in quantity, it can only be entered after the last of these ingredients before the quantity type "Ohhh."
8. Specifying the last ingredients to add to to obtain the required total of medicines or volume before August, a sign of some numerical uses the abbreviation "ad".
9. Instructions for pharmacies (Subscripti) for the manufacture of medicinal products, pharmaceutical form and quantity of the drug, indicating the weight or volume or operations of the unit and packaging type, written in Latin, using generally accepted abbreviations used in this provision in accordance with annex 6.
10. Instructions to the patient (Signature) on the use of medicines in a prescription written by Latvian language after the abbreviation "D.S.", went any where and how medication use.
11. If the recipe medicines manufactured and invoiced in question is urgent medical treatment person's article "the Other!". If the medicinal product in question immediately, the article "Status!". Mark desirable to specify a different color.
12. If the medicinal product is prohibited from replacing the medical person cross cross out the field "medicine allowed to be replaced".
13. All prescription form fields, in which case it is not intended to fill, treatment person cross cross out.
II. Conventional prescription form filling requirements 14. If medical treatment person when the usual recipe, provides for the possibility to choose between analogue, it indicates the number of halls, separated by the abbreviation "s." (Siva-or), and pharmacy in one of the medicine prescribed medications.
15. Diagnosis code indicating if the medicinal product is used repeatedly to recipes.
16. the period of validity of a Prescription treatment the person indicated for the diagnosis and izrakstāmaj.
17. The code or name of the medicinal product, the quantity (number of packages), price (one Pack), to pay the estimated amount (taking into account the number of packages) and the date of the prescription indicates a pharmacist or pharmacist Assistant, issuing the drug, this information confirms with a signature and a personal stamp.
18. the issue of medicines to be used repeatedly, the pharmacist or the pharmacist prescription Assistant recipes the other side made a reference to the medicinal product concerned, the quantity and the date of issue of the approval, the signature and personal stamp, and ensure that it would be possible to identify the Pharmacy where drugs have been issued.
III. Special prescription form filling requirements 19. E forms the way the doctor indicates if a recipe is discharged by another Member State of the European Union, Norway, Iceland, Liechtenstein or Switzerland's citizen under international treaty providing for mutual settlements for the health services.
20. The insurance companies as well as Kuma nosa compensation doctor indicates, if the acquisition of medicines the patient is compensated for by an insurance company.
21. the amount of State compensation doctor indicates, if the recipes extract medicinal product or medical device according to the stated refund policy.
22. If the recipes extract Glycemic teststrēmel's pregnant, the doctor in addition to the pamatdiagnoz code indicates code "Z33".
23. code for medicinal products granted the quantity (number of packages), price (one Pack), to pay the estimated amount (taking into account the number of packages), its distribution between the patient and other persons, as well as the date of issue of the notes or the pharmacist the pharmacist's Assistant, issuing the drug, confirming this information with signature, personal stamp and the stamp of the pharmacies. If the quantity is not to be served in full packages, package quantity indicates decimal numbers with precision up to four decimal places.
Health Minister g. Smith annex 4 of the Cabinet of Ministers of 8 March 2005, regulations No 175 drugs which form the usual recipes allowed to discharge more than three months long treatment course no PO box
Anatomic therapeutic chemical group exceptions (Hall on one of the recipes make allowed no more than three months for a long course of treatment) 1. Gastrointestinal tract and metabolism the 1.1.
Features functional gastrointestinal disorders (A03) of A03BA03 of the A03FA02 A03BA01 Atropin Hyoscyamin Cisaprid-1.2.
Features of liver disease and bile formation and hand disorders treatment (A05) 1.3.
Features treatment of diabetes (A10) 2. Blood and hematopoietic organs of 2.1.
Antitrombotisk funds (B01AC07 Dipyridamol) 3. Cardiovascular System 3.1.
Heart disease treatment vazodilatator be used (C01D) 3.2.
Agent features (C02) C02BA01 C02CC02 Guanethidin C02CC04 of Debrisoquin Trimetaphan is a 3.3 Diazoxid C02DA01
Diuretics (C03) 3.4.
Beta-blockers (C07) 3.5.
Calcium channel blockers (C08) C08EA02 C08EX01 Lidoflazin-3.6 Bepridil
Renin-angiotensin system (C09) features affecting 3.7.
Serum lipids reducing features (C10) C10AX02 C10AX04 C10AX09 Ezetimib to publicise the Probucol 4. Uro system and effects of 4.1.
The hormonal contraceptives for systemic use (G03) 4.2.
Estrogen (G03C, natural and pussintētisk) 4.3.
The combination of estrogen (Estriol Estrone, G03CC04 G03CC06) 4.4.
The lack of G03DA01 Gestonoron of G03DB02 (G03D) Megestrol G03DB04 Nomegestrol 4.5.
The lack and estrogen combination (G03F) G03FB03 Chlormadinon and Estrogen 4.6.
Uroloģisk features, including spazmolītisk funds (G04B) G04BE01 Alprostadil 5. Systemic hormone-containing features, except for the effects of insulin and 5.1.
Thyroid hormone-containing funds (H03) 5.2.
Antitireoīd funds (H03B) 5.3.
The hormone Antiparatireoīd (H05B) 6. Musculoskeletal System 6.1.
Anti-inflammatory and pretreimatism, not steroids (M01A, M01AB, M01AC, M01AG, M01AX, M01A) M01AA02 Mofebutazon is M01AX17 of 6.2 Nimesulid
Miorelaksant, Central operations (M03B) 6.3.
Pretpodagr (M04) M04AB03 Benzbromaron 7. Nervous System 7.1.
Pretmigrēn, alkaloids (N02C) 7.2.
Anti-epileptics (N03) Vigabatrin N03AX10 Felbamat N03AG04 4.5.
Pretparkinsonism (N04) and the Dop dop N04B derivatives 8. Respiratory System 8.1.
Features of obstructive respiratory diseases, adrenerģisk, delay (R03) R03AA01 R03AK01 a combination of Epinephrin Epinephrin 8.2.
Other features of obstructive respiratory diseases, delay (R03BB, R03BC, R03BX) 8.3.
Other features of obstructive respiratory diseases, systemic (R03D, R03DB, R03DX) R03DA04-R03DA74, R03DB04-Theophyllin Theophyllin combinations 9. Sensory organs in 9.1.
Pretglaukom and miotisk funds (S01) S01EA05 Brimonidin S01EB03 Ecothiopat S01EB04 Demecari of the S01EB08 Aceclidin of Health Minister g. Smith annex 5 of the Cabinet of Ministers of 8 March 2005, regulations No 175 to the illicit manufacture of narcotic drugs and psychotropic substances recognized as the maximum quantity authorised to be invoiced for one recipes no PO box
The international name of the substance, the maximum quantity of a substance that is allowed to make to recipes (g) notes 1.
Buprenorphine hydrochloride 0.224 2.
Ciklobarbitāl of 1.0 3.
Dihydrocodeine tartrate 6.72 4.
Etilmorfīn of 1.0 5.
A maximum of 10 0.084 fentanyl patches 6.
Codeine 0.3 7.
Metilfenidāt hydrochloride 0.6 8.
Morphine hydrochloride injection 0.4 solutions 9.
Morphine hydrochloride tablets 10 6.0.
Morphine sulphate 12.0 11.
Oxycodone 4.48 12.
Petidīn to 0.5 13.
Pentazocīn of 0.3 14.
The Health Minister Trimeperidīn 0.4 G. Buchanan annex 6 of the Cabinet of Ministers of 8 March 2005, regulations no common abbreviation used 175 no PO box
Full term in Latin abbreviation sign Latvian Edition 1.
acid acid, of the eye.
Add adds, added 3.
Ad I Medici of the ad to me. honey.
the doctor hands 4.
use of extern for us ad ad. Ext.
external use 5.
ad for ad of intern USA USA. int.
oral use 6.
use of ad USA of ad propriu. resources.
personal use 7.
ad ad of stained stained.
glass container 8.
aequal a aeq.
ampull amp., ampull.
Ana Ohhh similar parts, down 11.
of the anhydric anhydr.
Aqua destillat-aq. des.
distilled water 14.
butyr butyr Forum.
capsule of amylace caps. amyl.
starch capsule 17.
capsule of gelatinos caps. the gel.
gelatin capsule 18.
charts of cerat chart. hope.
the waxy paper 20.
charts the chart paraffinat. paraff.
paraffin paper 21.
concentrate in Conca.
concentrated in 22.
Da; Detur; Dentur D.
give; to be given; to be given in 26.
Da scatul d. in sc in.
go box 27.
Da in vitro d. in stained.
give a glass container, 28.
Da in vitro nigr D. in vitro nigr travels the dark container 29.
Da, Sign; Dentur, Signetur D.S.
DoD, represents; to get to is 30.
Some tales will go; Tales of Doss D.t.d. Dentur
giving a dose; to give the dose; the following dose issue 31.
decoct for dec.
dilut of dill.
divide in two. aequal in partes p. aeq.
sharing equal doses; sharing similar doses, 36.
give a d., DOS.
as the emulated emulsi emuls.
extract, extract 40.
extractum of extra fluid. FL.
liquid extract 41.
extractum sicc of extra. sicc.
dry extract 42.
extractum spiss for extra. spis.
thick extract 43.
Fiat (Fiano) (f).
to make to the top for the formation of 44.
the fruit of 47.
48 of gelatine.
globul in the globe.
the ball 49.
drop, drop 50.
the gtt gutts drops 51.
plants, grass, 52.
in the ampull in amp., ampull.
infus of inf.
in the capsule in caps.
55 the capsules.
in the in the obl oblat.
oblat in 56.
in the tabulett tab, in the table in.
of line, line liniment.
liquid liniment of ointment, 58.
liq liquor, liquid in.
liquid, liquid 59.
mass of 60.
Massa pilular m. of the Castle.
pea mass 61.
Misc; Misceatur M.
mix; to be mixed, blended 62.
Misc. Da. Sign; Misceatur, Signetur, Detur M.D.S.
mix, give, represents; to be mixed, given, indicated 63.
mix to the top 64.
65. the potion
mucilag a barrel.
Olea of the egg.
about partes, p.
part, part 69.
partes of the aequal p. aeq.
equal parts, the same (similar) went for 70.
pill, pilula Palace.
bean, snap peas, 72.
Pro injectionib Pro inj.
injection of 74.
Pro use the extern Pro USA. Ext.
exclusively use 75.
Pro USA intern Pro USA. int.
oral use 76.
powder of pulv., pulv
quantum satis q.s.
How need; the required quantity of 79.
the root of the 80 's.
repet, repetatur repeat.
Repeat; is repeated to 82.
saknen, ground trunk 83.
pretty enough to 84.
seeds of 85.
se, s Siva.
Sign, Signetur S.
represents; so is 88.
sirup in sir.
solution of 91.
spec to spec.
herbal tea 92.
spirits of the droppings.
sublimat in subl.
sublimēt is 94.
of subtilissim subtilis.
the finest of the 96.
suppositori of supp.
candles for 97.
of the supp rectal suppositori. Rec.
the rectal suppository rectal to 98.
of the vaginal supp suppositori. VAG.
vaginal rectal of the 99.
tabulett; tabuletta tab, table.
Tablet, 100 tablets.
Tales of t.
tinctur t-ra, tinc., tc.
unguents for ung.
of stained stained.
glass containers, container Health Minister g. Smith
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