Generic drug of Amlor
Therapeutic class: Cardiology and angiology
active ingredients: Amlodipine
laboratory: Teva Sante
Box of 90
All forms
Indication
Hypertension
Chronic stable angina
Vasospastic angina (Prinzmetal syndrome)
Dosage AMLODIPINE TEVA 5 mg Capsule Box of 90
Dosage
adults
For hypertension and angina, the usual starting dose is 5 mg AMLODIPINE TEVA once daily, which can be increased to a maximum dose of 10 mg depending on the patient's individual response.
In hypertensive patients, amlodipine has been used in combination with a thiazide diuretic, an alpha blocker, a beta-blocker, or an angiotensin converting enzyme inhibitor. In angina, amlodipine can be used alone or in combination with other antianginal agents in patients with nitrate-refractory angina and / or adequate doses of beta-blockers.
No dose adjustment of AMLODIPINE TEVA is necessary when coadministered with thiazide diuretics, beta-blockers and angiotensin converting enzyme inhibitors.
Special populations
Elderly
Amlodipine used at similar doses shows good equivalent tolerance in elderly patients and younger patients. Normal dosing regimens are recommended for elderly patients, but dosage increases should be made with caution (see Warnings and Precautions and Pharmacokinetic Properties sections).
Hepatic insufficiency
Dose recommendations have not been established in patients with mild to moderate hepatic impairment therefore the dose should be selected with caution and should start at the lowest effective dose (see sections Warnings and Precautions for Use). and pharmacokinetic properties ). The pharmacokinetic properties of amlodipine have not been studied in patients with severe hepatic impairment. Amlodipine should be started at the lowest dose and slowly increased in patients with severe hepatic impairment.
Renal failure
Changes in plasma concentrations of amlodipine are not correlated with the degree of renal impairment, so a usual dosage is recommended. Amlodipine is not dialysable.
Children and adolescents
Hypertensive children and adolescents from 6 to 17 years old.
The recommended oral antihypertensive dosage in children aged 6 to 17 years is 2.5 mg once daily as the initial dose, which can be increased to 5 mg once daily if the desired blood pressure is not reached after four weeks. Doses greater than 5 mg once daily have not been studied in pediatric patients (see sections Pharmacodynamic properties and Pharmacokinetic properties ).
A dosage of 2.5 mg amlodipine is not possible with this drug.
Children under 6 years old.
There is no data available.
Administration mode
Capsule for oral administration.
Against indications
Amlodipine is contraindicated in patients with:
· Hypersensitivity to dihydropyridine derivatives, amlodipine or any of the excipients.
· Severe hypotension.
· Shock (including cardiogenic shock)
· Obstruction of the left ventricular outflow tract (eg, high degree of aortic stenosis).
· Hemodynamically unstable heart failure after acute myocardial infarction.
Adverse effects Amlodipine Teva
Summary of the security profile
The most common side effects reported during treatment are drowsiness, dizziness, headache, palpitations, flushing, abdominal pain, nausea, swollen ants, edema, and fatigue.
List of undesirable effects
The following adverse reactions have been observed and reported during treatment with amlodipine at the following frequencies: very common (≥ 1/10); frequent (≥ 1/100 to <1/10); uncommon (≥ 1/1000 to ≤ 1/100); rare (≥ 1/10 000 to ≤ 1/1 000); very rare (≤1 / 10, 000).
In each frequency group, the adverse effects are presented in order of decreasing severity.
Class of organ systems | Frequency | Side effects |
Blood and lymphatic system disorders | Very rare | Leukocytopenia, thrombocytopenia, |
Immune system disorders | Very rare | Allergic reaction |
Metabolism and nutrition disorders | Very rare | hyperglycemia |
Psychiatric disorders | Rare | Insomnia, change of mood (including anxiety), depression |
Rare | Confusion | |
Nervous system disorders | Frequent | Drowsiness, dizziness, headache (especially at the beginning of treatment) |
Rare | Tremor, dysgeusia, syncope, hypoaesthesia, paresthesia | |
Very rare | Hypertonia, peripheral neuropathy | |
Eye disorders | Rare | Visual disorder (including, diplopia) |
Affections of the ear and labyrinth | Rare | tinnitus |
Heart conditions | Frequent | palpitations |
Very rare | Myocardial infarction, arrhythmia (including bradycardia, ventricular tachycardia, and atrial fibrillation) | |
Vascular disorders | Frequent | Flushing |
Rare | hypotension | |
Very rare | vasculitis | |
Respiratory, thoracic and mediastinal disorders | Rare | Dyspnea, rhinitis |
Very rare | Cough | |
Gastrointestinal disorders | Frequent | Abdominal pain, nausea |
Rare | Vomiting, dyspepsia, transit disorders (including diarrhea and constipation), dry mouth | |
Very rare | Pancreatitis, gastritis, gingival hyperplasia | |
Hepatobiliary disorders | Very rare | Hepatitis, jaundice, elevated liver enzymes * |
Skin and subcutaneous tissue disorders | Rare | Alopecia, purpura, change of skin color, hyperhidrosis, pruritus, rash, exanthema |
Very rare | Angioedema, erythema multiforme, urticaria, exfoliating dermatitis, Stevens-Johnson syndrome, angioedema, photosensitivity | |
Musculoskeletal, Connective Tissue and Bone Disorders | Frequent | Edema of the ankles |
Rare | Arthralgia, myalgia, muscle cramp, back pain | |
Renal and urinary disorders | Rare | Micturition disorder, nocturia, increased urinary frequency |
Disorders of reproductive organs and breast | Rare | Impotence, gynecomastia |
General disorders and administration site conditions | Frequent | Edema, tiredness |
Rare | Chest pain, asthenia, pain, discomfort | |
investigations | Rare | Increased weight, decreased weight |
* Generally suggestive of cholestasis
Exceptional cases of extrapyramidal syndrome have been reported.