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(Due to limited stock, please contact customer service before placing an order.) Japan Calvan Bevantolol (Bevantolol Hydrochloride) Calvan Tablets 25mg, 50mg, 100mg: 100 tablets. Slows heart rate, dilates peripheral blood vessels, and steadily lowers blood pressure. Antihypertensive medication. Stabilizes heart rate.

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HKD$900.00 – HKD$2,200.00Price range: HKD$900.00 through HKD$2,200.00
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描述

Direct Shipping from Overseas (Direct Shipping from Japan)

Calvin Tablets 25/50 mg/100 mg
Calvan® Tablets Bevantolol

Revised December 2025 (2nd Edition) / Revised July 2023 (1st Edition)
Category 872149 | Bevantrol Hydrochloride Preparations

Hypertension

Calvan Tablets

Admission, etc.

Tablet 25 YJ 2149036F1020 Approved 20700AMZ00433000 Sales began in June 1995
Calvan Tablets 25
Tablet 50 YJ 2149036F2026 Approved 20700AMZ00434000 Sales began in June 1995
Calvan Tablets 50
Tablet 100 YJ 2149036F3022 Approved 20700AMZ00435000 Sales began in June 1995
Calvan Tablets 100
Storage Instructions / Expiration Date Store at room temperature / 3 years
Regulatory Classification –
Manufacturing and Sales Yuan Chemifa Co., Ltd., Japan
2-2-3 Iwamotocho, Chiyoda Ward, Tokyo
Packaging 100 tablets each [10 tablets (PTP) × 10]
Shipping method Direct Shipping from Overseas (Direct Shipping from Japan) *Controlled Substances/Prescription Drugs: Must comply with local regulations
Preparation and shipping time Once payment and prescription eligibility have been verified, orders are typically shipped within 4 to 7 business days.

3. Composition and Properties

25 mg tablet

Active Ingredients:Each tablet contains 25.0 mg of bevantrol hydrochloride

Additive:Lactose hydrate, crystalline cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, hydrogenated oil, magnesium stearate, hydroxypropylmethylcellulose, polyethylene glycol 400, titanium dioxide, carnauba wax

Characteristics:White film-coated tablet, Identification: NC CG, φ6.1 mm / Thickness 2.9 mm / 80 mg

50 mg tablet

Active Ingredients:Each tablet contains 50.0 mg of bevantrol hydrochloride

Additive:Same as above (polyethylene glycol 400)

Characteristics:White film-coated tablet, Identification: NC CF, φ6.6 mm / Thickness 2.9 mm / 91.5 mg

100 mg tablet

Active Ingredients:Each tablet contains 100.0 mg of bevantrol hydrochloride

Additive:Same as above, with polyethylene glycol changed to 6000

Characteristics:White film-coated tablet with score line; Identification: NC CE; φ8.5 mm / Thickness 3.2 mm / 169 mg

C20H27NO4・HCl: Molecular weight 381.89; melting point 138–143°C; white crystals or crystalline powder; no optical activity.

Structural Formula

4./6./7. Efficacy and Effects; Dosage and Administration

Performance and Results:Hypertension

The usual adult dose is 100 mg of bevantrol hydrochloride per day, taken orally in two divided doses; if the effect is insufficient, the dose may be increased to 200 mg per day. The dose may be adjusted based on age and symptoms.

Chromaffin cell tumors or paragangliomas: Treatment with this product should be initiated only after treatment with an alpha-blocker has been started, and an alpha-blocker should be administered concomitantly throughout the course of treatment. [2.7] [9.1.4]

18. / 16. / 17. Pharmacology, Pharmacokinetics, and Clinical Aspects

It reduces heart rate through β₁ blockade and lowers blood pressure by dilating peripheral blood vessels via α₁ blockade and calcium channel blockade. No ISA. The β₁/β₂ selectivity ratio is approximately 11.5–32; the β₁/α₁ ratio is approximately 14; and the α₁/Ca antagonism ratio is approximately 4.

Single 100 mg dose in healthy adults: Tmax 0.75 ± 0.27 hr, Cmax 876 ± 297 ng/mL, T½α 1.36 ± 0.56 hr, T½β 9.7 ± 6.0 hr. The cumulative excretion rate of unchanged (free) drug in 48-hour urine was 0.591 TP3T. In 120-hour urine, 72.21 TP3T of ¹⁴C-labeled drug was excreted, and 15.01 TP3T was excreted in feces.

Single-dose plasma concentration

Domestic hypertension-related trials: 685 cases; overall response rate: 63.61 TP3T (decrease or greater): Mild to moderate essential hypertension: 62.01 TP3T (385/621); severe hypertension: 83.31 TP3T (30/36); hypertension with renal impairment: 75.01 TP3T (21/28).

2./8./9./10./11./13./14. Contraindications, Precautions, Interactions, Side Effects

2. Contraindications

  1. Diabetic ketoacidosis, metabolic acidosis (which may contribute to decreased systolic contractility, peripheral arterial dilation, and decreased blood pressure)
  2. Psychogenic Shock
  3. Congestive Heart Failure
  4. Right-sided heart failure caused by pulmonary hypertension
  5. Severe bradycardia (marked sinus bradycardia), second- or third-degree atrioventricular block, sinoatrial block
  6. Pregnant women or women who may be pregnant (reduced fetal body weight observed in rats) [9.5]
  7. Untreated pheochromocytoma or paraganglioma [7.] [9.1.4]

8. Patients receiving long-term treatment should undergo regular cardiac function tests. Reduce the dose or discontinue the medication in cases of bradycardia or hypotension; administer atropine sulfate if necessary. Sudden discontinuation of similar medications has been associated with worsening angina or myocardial infarction; therefore, the medication must be tapered off gradually. Avoid administration within 48 hours prior to surgery. Dizziness may occur; avoid driving or operating hazardous machinery during the initial phase of treatment.

9. Patients at risk of heart failure should use this medication in combination with cardiac glycosides and with caution. Patients at risk of bronchial asthma or bronchospasm (this product also has β₂-blocking effects). Patients with idiopathic hypoglycemia, poorly controlled diabetes, or those who have fasted for an extended period are prone to hypoglycemia, which may mask symptoms such as tachycardia. For patients with severe renal or hepatic impairment, treatment should be initiated at a low dose. Weigh the benefits against the risks during breastfeeding (the drug is excreted in rat milk). No clinical trials have been conducted in children. Elderly patients should start with a low dose (e.g., 50 mg/day).

10.2 Precautions for Concomitant Use:Sympatholytic agents such as Lixiping (bradycardia, decreased blood pressure); hypoglycemic agents such as insulin and tolbutamide (enhanced hypoglycemia and masking of hypoglycemic symptoms); calcium channel blockers such as verapamil (excessive blood pressure reduction, cardiac function suppression); clonidine (may increase the risk of rebound hypertension upon discontinuation; this drug should be temporarily discontinued before stopping clonidine); antiarrhythmic drugs such as disopyramide, procainamide, and ajmaline (excessive cardiac function suppression).

11.1 Serious Adverse Effects:Heart failure (less than 0.11 TP3T), atrioventricular block (less than 11 TP3T), sinus node dysfunction (frequency unknown); asthma attacks, dyspnea (frequency unknown).

11.2:Neurological (dizziness, headache, drowsiness, insomnia, etc.), renal (elevated BUN/creatinine), hepatic (elevated ALT/AST), cardiovascular (bradycardia, palpitations, decreased blood pressure, etc.), respiratory (cough, shortness of breath, wheezing), gastrointestinal system, skin rash, urinary abnormalities, elevated uric acid/total cholesterol/CK/potassium, edema, fatigue, decreased tear production, etc.

13. Excess:Possible bradycardia, heart failure, bronchospasm, or hypoglycemia. Discontinue the medication and perform gastric lavage as needed. Treat bradycardia with atropine sulfate or, if necessary, isoproterenol or glucagon; treat hypotension with epinephrine; treat acute heart failure with cardiac glycosides, diuretics, and oxygen; treat bronchospasm with isoproterenol or theophylline; treat hypoglycemia with glucose.

14. PTP tablets must be removed from the blister pack before taking them; if swallowed accidentally, they may pierce the esophagus or even cause a perforation.

22–26. Packaging, Inquiries, Manufacturing, and Sales

22. 25/50/100, 100 tablets each [10 tablets (PTP) × 10]

24. Chemifa Co., Ltd., Safety Management Department, 2-2-3 Iwamotocho, Chiyoda-ku, Tokyo 101-0032
TEL 0120-47-9321 / 03-3863-1225 FAX 03-3861-9567

26.1 Manufacturer and Distributor: Japan Chemifa Co., Ltd., 2-2-3 Iwamotocho, Chiyoda-ku, Tokyo

※ This page was translated by Hkeemall based on PMDA Package Insert 2149036F1020_1_17; it is not a substitute for a doctor’s prescription or the original Japanese version.
Enter "Calvan" in the PMDA "Package Insert Information" field to search for the original version.

[Disclaimer]

  1. The information regarding medications, treatments, or health management contained in this article is compiled from international authoritative medical journals and official clinical literature, and is intended for general science and educational reference only.
  2. The indications, side effects, and contraindications of related medications may vary depending on national regulations and individual physical conditions. Do not blindly take medication on your own or change your treatment plan.
  3. The author and publishing platform assume no legal liability for any medical delays, adverse reactions, or direct or indirect losses caused by the use of the information in this article. All medical decisions should be discussed with your attending physician before being made.

Additional information

Specifications

Calvan Tablets 25 mg, Calvan Tablets 50 mg, Calvan Tablets 100 mg

1 review for (貨源緊張下單前先聯繫客服)日本 Calvan Bevantolol 鹽酸貝凡洛爾 カルバン錠 25mg 50mg 100mg:100錠 減緩心率、擴張外周血管並平穩降壓 降壓藥 穩定心率

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