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Kuinopril Tablets

NAFDAC Reg. No. 04-9631 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 30 October 2026 · synced automatically from official sources.
Producto
Kuinopril Tablets
Número NAFDAC
04-9631
Principio activo
Lisinopril
Dosis
10 mg
Forma
Tablet
Tamaño del envase
3 x 10's (in PVC-Alu blisters)
Fabricante
No Constan
Solicitante (titular)
Drugfield Pharmaceuticals Limited
Approved
7 May 2021
Estado
Inactive Ver en NAFDAC ↗
Registro válido hasta
6 May 2026
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Lisinopril: uses, dosage and brands worldwide

Lo que encontramos

  • Kuinopril Tablets is on the NAFDAC register with an active registration (04-9631). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Kuinopril Tablets

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Advertencia grave: FETAL TOXICITY See full prescribing information for complete boxed warning. When pregnancy is detected, discontinue lisinopril as soon as possible. ( 5.1 ) Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. ( 5.1 ) WARNING: FETAL TOXICITY When pregnancy is detected, discontinue lisinopril as soon as possible [see WARNINGS AND PRECAUTIONS ( 5.1 )] . …
Para quién es

Lisinopril tablet USP is an angiotensin converting enzyme (ACE) inhibitor indicated for: Treatment of hypertension in adults and pediatric patients 6 years of age and older ( 1.1 ) Adjunct therapy for heart failure ( 1.2 ) Treatment of Acute Myocardial Infarction ( 1.3 ) 1.1 Hypertension Lisinopril tablet USP is indicated for the treatment of hypertension in adult patients and pediatric patients 6 years of age and older to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. …

Cómo tomarlo y con qué frecuencia
  • Hypertension: Initial adult dose is 10 mg once daily
  • Titrate up to 40 mg daily based on blood pressure response
  • Initiate patients on diuretics at 5 mg once daily
  • Pediatric patients with glomerular filtration rate > 30 mL/min/1.73m 2 : Initial dose in patients 6 years of age and older is 0.07 mg per kg (up to 5 mg total) once daily Heart Failure: Initiate with 5 mg once daily
  • Increase dose as tolerated to 40 mg daily Acute Myocardial Infarction (MI): Give 5 mg within 24 hours of MI
  • Followed by 5 mg after 24 hours, then 10 mg once daily Renal Impairment: For patients with creatinine clearance > 10 mL/min and < 30 mL/min, halve usual initial dose
  • For patients with creatinine clearance < 10 mL/min or on hemodialysis, the recommended initial dose is 2.5 mg Hypertension Initial Therapy
  • In adults: The recommended initial dose is 10 mg once a day
  • Dosage should be adjusted according to blood pressure response
  • The usual dosage range is 20 mg to 40 mg per day administered in a single daily dose
  • Doses up to 80 mg have been used but do not appear to give greater effect
  • Use with Diuretics
  • In Adults If blood pressure is not controlled with lisinopril alone, a low dose of a diuretic may be added (e.g, hydrochlorothiazide, 12.5 mg)
  • After the addition of a diuretic, it may be possible to reduce the dose of lisinopril
Fortalezas en las que viene

Tablets: 2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg ( 3 ) 2.5 mg tablet is a white to off-white, round, biconvex, uncoated tablet with "LUPIN" debossed on one side and "2.5" on other side. 5 mg tablet is a pink coloured, round, biconvex, uncoated tablet with "5" debossed on one side and breakline on other side. …

Infancia
  • Antihypertensive effects and safety of lisinopril have been established
  • In pediatric patients aged 6 to 16 years [see DOSAGE AND ADMINISTRATION and CLINICAL STUDIES ]
  • No relevant differences between the adverse reaction profile for pediatric patients and adult patients were identified
  • Safety and effectiveness of lisinopril have not been established
  • In pediatric patients under the age 6 or in pediatric patients with glomerular filtration rate < 30 mL/min/1.73 m 2 [see DOSAGE AND ADMINISTRATION , CLINICAL PHARMACOLOGY , and CLINICAL STUDIES ] . …
Older adults

No dosage adjustment with lisinopril is necessary in elderly patients. In a clinical study of lisinopril in patients with myocardial infarctions (GISSI-3 Trial) 4,413 (47%) were 65 and over, while 1,656 (18%) were 75 and over. In this study, 4.8 % of patients aged 75 years and older discontinued lisinopril treatment because of renal dysfunction vs. 1.3% of patients younger than 75 years. …

While you are taking it
  • NOTE: This information is intended to aid in the safe and effective use of this medication
  • It is not a disclosure of all possible adverse or intended effects
  • Pregnancy Advise pregnant women and females of reproductive potential of the potential risk to a fetus
  • Advise females of reproductive potential to notify their healthcare provider with a known or suspected pregnancy [see WARNINGS AND PRECAUTIONS and USE IN SPECIFIC POPULATIONS ]
  • Angioedema Angioedema, including laryngeal edema may occur at any time during treatment with angiotensin converting enzyme inhibitors, including lisinopril. …
Talk to a doctor first if
  • Angioedema or a history of hereditary or idiopathic angioedema Hypersensitivity Co-administration of aliskiren with lisinopril in patients with diabetes Lisinopril is contraindicated in combination with a neprilysin inhibitor (e.g., sacubitril)
  • Do not administer Lisinopril tablet USP within 36 hours of switching to or from sacubitril/valsartan, a neprilysin inhibitor [see WARNINGS and PRECAUTIONS ]. …
Medicines it may not mix with

Diuretics: Excessive drop in blood pressure ( 7.1 ) NSAIDS: Increased risk of renal impairment and loss of antihypertensive efficacy ( 7.3 ) Dual inhibition of the renin-angiotensin system: Increased risk of renal impairment, hypotension and hyperkalemia ( 7.4 ) Lithium: Symptoms of lithium toxicity ( 7.5 ) Gold: Nitritoid reactions have been reported ( 7.6 ) Concomitant mTOR inhibitor or neprilysin inhibitor use may increase angioedema risk ( 7.7 , 7.8 ) 7.1 Diuretics Initiation of lisinopril in patients on diuretics may result in excessive reduction of blood pressure. …

Warnings

Angioedema: Discontinue lisinopril, provide appropriate therapy and monitor until resolved ( 5.2 ) Renal impairment: Monitor renal function periodically ( 5.3 ) Hypotension: Patients with other heart or renal diseases have increased risk, monitor blood pressure after initiation ( 5.4) Hyperkalemia: Monitor serum potassium periodically ( 5.5 ) Cholestatic jaundice and hepatic failure: Monitor for jaundice or signs of liver failure ( 5.6 ) 5.1 Fetal Toxicity Lisinopril can cause fetal harm when administered to a pregnant woman. …

Posibles efectos secundarios

Common adverse reactions (events 2% greater than placebo) by use: Hypertension: headache, dizziness and cough ( 6.1 ) Heart Failure: hypotension and chest pain ( 6.1 ) Acute Myocardial Infarction: hypotension ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Lupin Pharmaceuticals, Inc. at 1-800-399-2561 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Lisinopril can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. …

If you take too much

Following a single oral dose of 20 g/kg no lethality occurred in rats, and death occurred in one of 20 mice receiving the same dose. The most likely manifestation of overdosage would be hypotension, for which the usual treatment would be intravenous infusion of normal saline solution. Lisinopril can be removed by hemodialysis [see CLINICAL PHARMACOLOGY ( 12.3 )] .

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2023-08-18.

Label for lisinopril, the active ingredient registered with NAFDAC.

Check your pack of Kuinopril Tablets

Add the expiry date on your pack for a full Trust Score.

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Kuinopril Tablets

What is in Kuinopril Tablets?

Kuinopril Tablets contains Lisinopril (10 mg), as tablet, according to its NAFDAC registration record.

Is Kuinopril Tablets registered with NAFDAC?

Yes. Kuinopril Tablets is listed on the NAFDAC register under registration number 04-9631, and its registration is active as of 30 October 2026.

Has Kuinopril Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Kuinopril Tablets in our automatically synced alert list.

How can I check that my pack of Kuinopril Tablets is genuine?

Run a free authenticity scan with the NAFDAC number 04-9631, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Kuinopril Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Hypertension: Initial adult dose is 10 mg once daily. Titrate up to 40 mg daily based on blood pressure response. Initiate patients on diuretics at 5 mg once daily ( 2.1 ) Pediatric patients with glomerular filtration rate > 30 mL/min/1.73m 2 : Initial dose in patients 6 years of age and older is 0.07 mg per kg (up to 5 mg total) once daily ( 2.1 ) Heart Failure: Initiate with …

What is Kuinopril Tablets used for?

Lisinopril tablet USP is an angiotensin converting enzyme (ACE) inhibitor indicated for: Treatment of hypertension in adults and pediatric patients 6 years of age and older ( 1.1 ) Adjunct therapy for heart failure ( 1.2 ) Treatment of Acute Myocardial Infarction ( 1.3 ) 1.1 Hypertension Lisinopril tablet USP is indicated for the treatment of hypertension in adult patients and pediatric patients 6 (Summarised from the official U.S. FDA label for lisinopril. Always follow your doctor or pharmacist.)

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