|...||...||...||Active substance||Medicinal product name||Pharmaceutical form||Strength||ATC code||Max. price range (€ incl. VAT)|
|Is available (according to the information provided by wholesalers)||Prescription (Pr.)||Mucosa nasalis suis, Mucosa oris suis, Mucosa pulmonis suis, Mucosa oculi suis, Mucosa vesicae felleae suis, Mucosa vesicae urinariae suis, Mucosa pylori suis, Mucosa duodeni suis, Mucosa oesophagi suis, Mucosa jejuni suis, Mucosa ilei suis, Mucosa coli suis, Mucosa recti suis, Mucosa ductus choledochi suis, Ventriculus suis, Pancreatis suis, Argenti nitras, Atropa belladonna, Oxalis acetosella, Semecarpus anacardium, Phosphorus, Lachesis mutus, Cephaelis ipecacuanha, Nux vomica, Veratrum album, Pulsatilla nigricans, Kreosotum, Sulfur, Natrium diethyloxalaceticum, Bacterium Coli-Nosode, Marsdenia condurango, Kalium bichromicum, Hydrastis canadensis, Mandragora e radice siccato, Momordica balsamina, Ceanothus americanus||Mucosa compositum solution for injection||Solution for injection||
Is available (according to the information provided by wholesalers)
|V03AX — ALL OTHER THERAPEUTIC PRODUCTS||€ 33.90–197.09||skatīt informāciju par zālēm un iepakojumiem|
Medicinal Product Register of Latvia contains information only about those substances and methods, that are prohibited for use in sport and are included in World Anti-doping agency’s Prohibited list. The Register contains information only about those Medicinal Products, which can be purchased in Latvia. The Register does not contain information about food supplements.
If You search in the Medicinal Product Register of Latvia and do not find the necessary information about use in sports, it does not mean that use of substance or method in sport is not prohibited.
Information about use in sports to Medicinal Product Register of Latvia is provided by Anti-doping bureau of Latvia. Information for use in sports is included for information purposes, it is not considered as an authoritative information on the status of the substance or method for use in sports. Anti-doping bureau of Latvia shall make all reasonable efforts to provide up-to-date and accurate information but does not accept liability for errors or omissions. Please be informed that there may be special circumstances or situations that require a doctor’s or pharmacist’s consultation. Please note that information about new products or changes in Prohibited list shall be renewed after accession of these products in the register or publication of the Prohibited list on the World Anti-Doping Agency’s website.
The purpose of the Meds75+ database of medication for older persons is to support the clinical decision-making on the pharmacotherapy of patients over 75 years of age and to improve medication safety in primary health care. The database contains classification and recommendation for almost 500 substance or their combination when used in older persons.
The Meds75+ database is maintained by the Finnish Medicines Agency, Fimea. Information regarding the use of medicinal products in persons over the age of 75 has been included in the register only for informative purposes. Patients should talk to their doctor before using medicinal products. The State Agency of Medicines does not take responsibility for the accuracy and completeness of this information. If you note any errors, please contact email@example.com.
Content of the database
Like in other health care databases, the medicinal substances are classified into categories A, B, C and D. The category indicates how suitable the medicinal substance is for persons over 75 years of age. The categories are based on a multidisciplinary clinical consensus.
The legend for each pharmaceutical substance contains information on the effects and dosing of the substance and the most typical adverse reactions and interactions. The legend does not contain indications or contraindications.
Using the database in health care
The database is primarily intended for physicians and other health care professionals. It must be borne in mind that individual cases might require the use of category D medicinal products. The pharmacotherapy must be started, changed or discontinued under the supervision of a physician.