Translations:Angiotensin II receptor blocker/33/en: Difference between revisions

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Message definition (Angiotensin II receptor blocker)
|-
| [[Valsartan]]
| Diovan
| 6
| 2–4 hrs
| 95%
| 25%
| 30/70%
| Yes
| 80–320
| Substrates: [[Multidrug resistance-associated protein 2|MRP2]] and [[OATP1B1|OATP1B1/SLCO1B1]]
|-
| [[Irbesartan]]
| Avapro
| 11–15
| 1.5–2 hrs
| 90–95%
| 70%
| 20/80%
| No
| 150–300
| Minor substrates of [[CYP2C9]]
|-
| [[Telmisartan]]
| Micardis
| 24
| 0.5–1 hr 
| >99%
| 42–58%
| 1/99%
| No
| 40–80
| None known; >97% via biliary excretion
|-
| [[Eprosartan]]
| Teveten
| 5
| 1–2 hrs 
| 98%
| 13%
| 30/70%
| No
| 400–800
| None known; >90% via renal and biliary excretion
|-
| [[Olmesartan]]
| Benicar/Olmetec
| 14–16
| 1–2 hrs 
| >99%
| 29%
| 40/60%
| No
| 10–40
| Substrates of [[OATP1B1|OATP1B1/SLCO1B1]]
|-
| [[Azilsartan]]
| Edarbi
| 11
| 1.5–3 hrs 
| >99%
| 60%
| 55/42%
| No
| 40–80
| Minor substrates of CYP2C9 
|-
| [[Fimasartan]]
| Kanarb
| 7–11
| 0.5–3 hrs after dosing.
| >97%
| 30–40%
| –
| –
| 30–120
| None known; primarily biliary excretion 
|-
! Drug
! Trade name
! [[Biological half-life]] [hrs]
! [[Cmax_(pharmacology)|Peak plasma concentration [Tmax] ]]
! [[Protein binding]] [%]
! [[Bioavailability]] [%]
! Renal/hepatic [[Clearance (medicine)|clearance]] [%]
! Food effect
! Daily dosage [mg]
! [[Metabolism]]/[[Transport protein|transporter]]
|}

|- | Valsartan | Diovan | 6 | 2–4 hrs | 95% | 25% | 30/70% | Yes | 80–320 | Substrates: MRP2 and OATP1B1/SLCO1B1 |- | Irbesartan | Avapro | 11–15 | 1.5–2 hrs | 90–95% | 70% | 20/80% | No | 150–300 | Minor substrates of CYP2C9 |- | Telmisartan | Micardis | 24 | 0.5–1 hr | >99% | 42–58% | 1/99% | No | 40–80 | None known; >97% via biliary excretion |- | Eprosartan | Teveten | 5 | 1–2 hrs | 98% | 13% | 30/70% | No | 400–800 | None known; >90% via renal and biliary excretion |- | Olmesartan | Benicar/Olmetec | 14–16 | 1–2 hrs | >99% | 29% | 40/60% | No | 10–40 | Substrates of OATP1B1/SLCO1B1 |- | Azilsartan | Edarbi | 11 | 1.5–3 hrs | >99% | 60% | 55/42% | No | 40–80 | Minor substrates of CYP2C9 |- | Fimasartan | Kanarb | 7–11 | 0.5–3 hrs after dosing. | >97% | 30–40% | – | – | 30–120 | None known; primarily biliary excretion |- ! Drug ! Trade name ! Biological half-life [hrs] ! Peak plasma concentration [Tmax] ! Protein binding [%] ! Bioavailability [%] ! Renal/hepatic clearance [%] ! Food effect ! Daily dosage [mg] ! Metabolism/transporter |}