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Cardace (Ramipril)

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Cardace is a moderately priced drug used alone or together with other medicines to treat high blood pressure. This drug is slightly more popular than comparable drugs. It is available in brand and generic form. Cardace is covered by most Medicare and insurance plans, but some pharmacy coupons or cash prices may be lower.

Other names for this medication:
Amprilan, Cardace, Cotriatec, Delix, Idroquark, Meramyl, Piramil, Pramace, Ramace, Ramasar, Ramibasics, Ramicard, Ramiclair, Ramicor, Ramifin, Ramigamma, Ramilich, Ramimed, Ramiplus, Ramipril, Ramiprilum, Ramzid, Ranid, Triatec, Tritace, Tritazide, Vesdil

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Also known as: Ramipril


Cardace is a perfect remedy in struggle against high blood pressure or decreasing the risk of heart attack, stroke, and death in certain patients. Cardace acts by relaxing blood vessels. It is an angiotensin-converting enzyme (ACE) inhibitor. Cardace is also known as Ramipril, Cardace, Tritace, Ramace, Lopace. Generic name of Cardace is Ramipril Tablets. Brand name of Cardace is Cardace.


Usual Adult Dose for Diabetic Nephropathy:

Initial dose: 2.5 mg orally once a day for patients not receiving a diuretic Maintenance dose: 2.5 to 20 mg/day orally in 1 to 2 divided doses

Usual Adult Dose for Hypertension:

Initial dose: 2.5 mg orally once a day for patients not receiving a diuretic Maintenance dose: 2.5 to 20 mg/day orally in 1 to 2 divided doses

Usual Adult Dose for Congestive Heart Failure:

Initial dose: 2.5 mg orally twice a day Maintenance dose: 5 mg orally twice a day

Usual Adult Dose for Left Ventricular Dysfunction:

Initial dose: 2.5 mg orally twice a day Maintenance dose: 5 mg orally twice a day

Usual Adult Dose for Myocardial Infarction:

Initial dose: 2.5 mg orally twice a day Maintenance dose: 5 mg orally twice a day

Detailed Cardace dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Cardace are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not use Cardace if you are allergic to ramipril, or if:

you recently took a heart medicine called sacubitril; or you have ever had a severe allergic reaction to any ACE inhibitor (benazepril, captopril, enalapril, fosinopril, lisinopril, moexipril, perindopril, quinapril, or trandolapril).

Do not take Cardace within 36 hours before or after taking medicine that contains sacubitril (such as Entresto).

If you have diabetes, do not use ramipril together with any medication that contains aliskiren (a blood pressure medicine).

You may also need to avoid taking ramipril with aliskiren if you have kidney disease.

To make sure Cardace is safe for you, tell your doctor if you have ever had:

kidney disease (or if you are on dialysis); an electrolyte imbalance (such as high levels of potassium in your blood); liver disease; a connective tissue disease such as Marfan syndrome, Sjogren's syndrome, lupus, scleroderma, or rheumatoid arthritis; if you are on a low-salt diet; or if you are also taking telmisartan (Micardis).

Do not use if you are pregnant. If you become pregnant, stop taking this medicine and tell your doctor right away. Cardace can cause injury or death to the unborn baby if you take the medicine during your second or third trimester.

You should not breast-feed while you are using ramipril.

Cardace is not approved for use by anyone younger than 18 years old.

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A tertiary care surgical intensive care unit in a university teaching hospital. Recurrent intravenous leiomyoma extending to the right heart chambers is extremely rare. As sensory responses are elicited in the majority of asymptomatic subjects and as the range of motion (ROM) is often limited during neurodynamic testing, it is questionable whether the elevation of the shoulder girdle would be absent in asymptomatic subjects. Laboratory data including tumour markers were within normal limits. We measured the distance between A and B in millimetres (mm) and determined the accuracy of the injections. Subchronic administration of SIECm reduced levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in animals treated with 100mg/kg and serum triglyceride levels at 400 and 1000mg/kg. Intervention design and assessment tools need to be strengthened in intervention studies with cooking components. We examined NF1 in 50 patients with MDS including 9 who had progressed to more advanced stages and 16 to acute leukemia. The dimensions of right and left maxillary sinuses of 30 subjects from plain CT were measured using SYNGO software and statistical analysis was done.

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Moderate alcohol consumption during different age intervals during adolescence and early adulthood was not associated with mammographic density in premenopausal women. Supersensitive detection of prostate-specific antigen in lyophilisation-concentrated serum. The investigation of other functions, such as being a vasovagal inhibitory, may shed stronger light on the functions of yawning. These interrelationships between loci at the phenotypic level raise the question of whether they evolve independently. Here, we report BMV can systemically infect rice (Oryza sativa var. Arthrogryposis is associated with over 400 medical conditions and 350 known genes with considerable variability in phenotypic expression. MRI may facilitate the diagnosis in uncertain cases with noncalcified or partially calcified lesions by showing the characteristic multivesicular structure, necrotic areas and proximity to vascular structures. The presence of adhesions and inflammation due to antecedent acute pancreatitis, difficult location of the bleeding site and breach in the posterior wall of stomach pose significant challenges during the surgical management. UCN-01 can be administered safely as an initial 72-hour CIV with subsequent monthly doses administered as 36-hour infusions. Removal of the IUD in such a situation has been recommended because of the risk of complication, such as fistula formation and colonic perforation.

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