TRIPLIXAM

This brand name is authorized in Brazil, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, Tunisia, Turkey.

Active ingredients

The drug TRIPLIXAM contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII TFT5IM1KGB - PERINDOPRIL ARGININE
 

Perindopril is an inhibitor of the enzyme that converts angiotensin I into angiotensin II (Angiotensin Converting Enzyme ACE). The converting enzyme, or kinase, is an exopeptidase that allows conversion of angiotensin I into the vasoconstrictor angiotensin II as well as causing the degradation of the vasodilator bradykinin into an inactive heptapeptide. Inhibition of ACE results in a reduction of angiotensin II in the plasma, which leads to increased plasma renin activity (by inhibition of the negative feedback of renin release) and reduced secretion of aldosterone. Since ACE inactivates bradykinin, inhibition of ACE also results in an increased activity of circulating and local kallikrein-kinin systems (and thus also activation of the prostaglandin system).

 
Read more about Perindopril
2
UNII F089I0511L - INDAPAMIDE
 

Indapamide is a sulfonamide derivative with an indole ring, pharmacologically related to thiazide diuretics, which acts by inhibiting the reabsorption of sodium in the cortical dilution segment. It increases the urinary excretion of sodium and chlorides and, to a lesser extent, the excretion of potassium and magnesium, thereby increasing urine output and having an antihypertensive action.

 
Read more about Indapamide
3
UNII 1J444QC288 - AMLODIPINE
 

Amlodipine is a calcium ion influx inhibitor of the dihydropyridine group (slow channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac and vascular smooth muscle.

 
Read more about Amlodipine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TRIPLIXAM Film-coated tablet MPI, EU: SmPC Health Sciences Authority (SG)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
C09BX01 C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09B ACE inhibitors, combinations → C09BX ACE inhibitors, other combinations
Discover more medicines within C09BX01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 531320100011507, 531320100011607, 531320100011707, 531320100011807
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 2490-MEE-1216, 2571-MEE-0217, 2573-MEE-0217, 2791-MEE-0617
EE Ravimiamet 1587876, 1587887, 1587898, 1587900, 1587911, 1587922, 1587933, 1587944, 1587955, 1587966, 1587977, 1587988, 1587999, 1588002, 1588013, 1588024, 1588035, 1588046, 1588057, 1588068, 1588079, 1588080, 1588091, 1588103, 1588114, 1650844, 1650877, 1650888, 1650901, 1650912, 1762006, 1762017, 1762028, 1762039, 1762040, 1762051, 1762062, 1762073
FI Lääkealan turvallisuus- ja kehittämiskeskus 042343, 449541, 460681, 479448, 494861, 502777, 562053, 590176
FR Base de données publique des médicaments 61442104, 62500731, 66643919, 69880873
HK Department of Health Drug Office 65989, 65990, 65991, 65992
HR Agencija za lijekove i medicinske proizvode HR-H-175417914, HR-H-385858036, HR-H-826085198, HR-H-919762076
LT Valstybinė vaistų kontrolės tarnyba 1066867, 1066868, 1066869, 1066870, 1072878, 1072879, 1072880, 1072881, 1072882, 1072883, 1072884, 1072885, 1072886, 1072887, 1072888, 1072889, 1072890, 1072891, 1072892, 1072893, 1072894, 1072895, 1072896, 1072897, 1072898, 1073715, 1073716, 1073717, 1073718, 1073719, 1084848, 1084849, 1084850, 1084851, 1084852, 1084853, 1084854, 1084855
MT Medicines Authority MA066/02002, MA066/02003, MA066/02004, MA066/02005
NL Z-Index G-Standaard, PRK 116173, 116181, 116203, 116211
PL Rejestru Produktów Leczniczych 100314971, 100314994, 100315019, 100315048
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W61001001, W61001002, W61001003, W61001004, W61001005, W61001006, W61001007, W61001008, W61002001, W61002002, W61002003, W61002004, W61002005, W61002006, W61002007, W61002008, W61003001, W61003002, W61003003, W61003004, W61003005, W61003006, W61003007, W61003008, W61004001, W61004002, W61004003, W61004004, W61004005, W61004006, W61004007, W61004008
SG Health Sciences Authority 15010P, 15011P, 15012P, 15013P, 15014P
TN Direction de la Pharmacie et du Médicament 9254201, 9254202, 9254203, 9254204
TR İlaç ve Tıbbi Cihaz Kurumu 8699552090823, 8699552090830, 8699552090847, 8699552090854

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