Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Olmesartan medoxomil
Drug ID BADD_D01603
Description Olmesartan belongs to the angiotensin II receptor blocker (ARB) family of drugs, which also includes [telmisartan], [candesartan], [losartan], [valsartan], and [irbesartan]. ARBs selectively bind to angiotensin receptor 1 (AT1) and prevent the protein angiotensin II from binding and exerting its hypertensive effects, which include vasoconstriction, stimulation and synthesis of aldosterone and ADH, cardiac stimulation, and renal reabsorption of sodium, among others. Overall, olmesartan's physiologic effects lead to reduced blood pressure, lower aldosterone levels, reduced cardiac activity, and increased excretion of sodium. Olmesartan also affects the renin-angiotensin aldosterone system (RAAS), which plays an important role in hemostasis and regulation of kidney, vascular, and cardiac functions. Pharmacological blockade of RAAS via AT1 receptor blockade inhibits negative regulatory feedback within RAAS, which is a contributing factor to the pathogenesis and progression of cardiovascular disease, heart failure, and renal disease. In particular, heart failure is associated with chronic activation of RAAS, leading to inappropriate fluid retention, vasoconstriction, and ultimately a further decline in left ventricular function. ARBs have been shown to have a protective effect on the heart by improving cardiac function, reducing afterload, increasing cardiac output and preventing ventricular hypertrophy and remodelling.[A174154] By comparison, the angiotensin-converting enzyme inhibitor (ACEi) class of medications (which includes drugs such as [ramipril], [lisinopril], and [perindopril]) inhibit the conversion of angiotensin I to angiotensin II through inhibition of the ACE enzyme. However, this does not prevent the formation of all angiotensin II within the body. The angiotensin II receptor blocker (ARB) family of drugs unique in that it blocks all angiotensin II activity, regardless of where or how it was synthesized. Olmesartan is commonly used for the management of hypertension and Type 2 Diabetes-associated nephropathy, particularly in patients who are unable to tolerate ACE inhibitors. ARBs such as olmesartan have been shown in a number of large-scale clinical outcomes trials to improve cardiovascular outcomes including reducing risk of myocardial infarction, stroke, the progression of heart failure, and hospitalization.[A174124,A178153,A173869,A185324,A185327,A185333,A185342,A185345] Like other ARBs, olmesartan blockade of RAAS slows the progression of diabetic nephropathy due to its renoprotective effects.[A185906,A185909,A185912] Orally available olmesartan is produced as the prodrug olmesartan medoxomil which is rapidly converted _in vivo_ to the pharmacologically active olmesartan.[A175330] It was developed by Daiichi Sankyo Pharmaceuticals and approved in 2002.[A175345, L5560]
Indications and Usage For the treatment of hypertension.
Marketing Status Prescription
ATC Code C09CA08
DrugBank ID DB00275
KEGG ID D01204
MeSH ID D000068557
PubChem ID 130881
TTD Drug ID D07UBG
NDC Product Code 33342-180; 67877-447; 0527-2425; 49252-066; 70771-1061; 70518-2127; 66039-944; 50228-341; 64552-4028; 62332-132; 33342-178; 33342-179; 65597-103; 66003-101; 71335-0999; 65841-168; 46708-133; 63629-8525; 68554-0069; 65862-742; 51407-198; 62332-133; 42291-542; 57664-755; 65372-1171; 71205-458; 13668-249; 68180-725; 64220-123; 65862-741; 71205-172; 52038-003; 70518-2347; 70771-1059; 71335-0197; 52562-011; 66003-104; 68180-726; 68382-643; 0527-2426; 70771-1060; 50090-4451; 68462-438; 63629-8523; 68382-644; 46708-132; 49252-065; 71335-1920; 65862-743; 68462-437; 16729-320; 63629-8524; 12666-0021; 57664-757; 70756-808; 42291-543; 14501-0011; 72189-137; 60505-4654; 63629-8522; 68462-436; 65597-104; 62331-056; 50228-339; 51407-199; 13668-248; 49252-067; 71205-459; 71335-1074; 71205-174; 70756-810; 16729-321; 50090-3655; 67877-445; 65862-708; 60505-4653; 67877-446; 46708-131; 50090-3656; 65015-676; 13668-250; 46708-849; 65691-0071; 51407-197; 71335-0817; 66003-103; 66039-824; 62512-0034; 38779-3064; 68180-724; 72189-138; 65597-101; 42571-202; 42571-201; 62332-131; 57664-756; 49587-110; 70756-809; 71335-0775; 68382-645; 50228-340; 0527-2427; 66577-019; 16729-322; 15894-0019; 42571-203; 50090-3487; 42291-544; 50090-3471; 52038-006; 60505-4652
Synonyms Olmesartan Medoxomil | Medoxomil, Olmesartan | 5-Methyl-2-oxo-1,3-dioxolen-4-yl)methoxy-4-(1-hydroxy-1-methylethyl)-2-propyl-1-(4-(2-(tetrazol-5-yl)phenyl)phenyl)methylimidazol-5-carboxylate - T287346 | Benicar | Olmetec | CS 866 | CS-866 | CS866 | Votum
Chemical Information
Molecular Formula C29H30N6O6
CAS Registry Number 144689-63-4
SMILES CCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NNN=N4)C(=O)OCC5=C(OC(=O)O5)C)C(C)(C)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal pain07.01.05.002--
Alopecia23.02.02.001--
Anaphylactic reaction10.01.07.001; 24.06.03.006--
Angioedema23.04.01.001; 10.01.05.009--Not Available
Arthralgia15.01.02.001--
Arthritis15.01.01.001--
Asthenia08.01.01.001--Not Available
Back pain15.03.04.005--
Blood bilirubin13.03.01.040--Not Available
Blood bilirubin increased13.03.01.008--
Blood creatine phosphokinase increased13.04.01.001--
Blood creatinine increased13.13.01.004--
Blood triglycerides increased13.12.03.001--Not Available
Blood uric acid increased13.02.04.001--Not Available
Bone pain15.02.01.001--
Bronchitis22.07.01.001; 11.01.09.001--
Chest pain22.02.08.003; 08.01.08.002; 02.02.02.011--Not Available
Cough22.02.03.001--
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.001--
Dizziness17.02.05.003; 02.01.02.004; 24.06.02.007--
Dyspepsia07.01.02.001--
Face oedema23.04.01.004; 08.01.07.003; 10.01.05.002--
Fatigue08.01.01.002--
Gastroenteritis11.01.07.004; 07.19.03.001--Not Available
Gastrointestinal pain07.01.05.005--
Haematuria24.07.01.047; 20.02.01.006--
Haemoglobin decreased13.01.05.003--Not Available
Headache17.14.01.001--
Hypercholesterolaemia14.08.01.001--Not Available
The 1th Page    1 2 3    Next   Last    Total 3 Pages