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Minocycline hydrochloride capsule (Meiman)

This product is applicable to the following infections caused by pathogens sensitive to this product, such as Staphylococcus, Streptococcus, pneumococcus, Neisseria gonorrhoeae, Shigella, Escherichia coli, Klebsiella, proteus, Pseudomonas aeruginosa, Treponema pallidum and Chlamydia: 1. Urethritis, male nongonococcal urethritis (NGU), prostatitis, gonorrhea, cystitis, epididymitis, intrauterine infection, pyelonephritis, pyelonephritis, pyelonephritis, cystitis, etc. 2. Superficial suppurative infection: acne, tonsillitis, scapulohumeral periarthritis, folliculitis, pyoderma, furuncle, furuncle, carbuncle, cellulitis, sweat gland, sebaceous cyst powder tumor, papillary dermatitis, paronychia, abscess, secondary infection of corns, pharyngitis, dacryocystitis, blepharitis, wheat granuloma, gingivitis, pericoronitis, dental maxillary sinusitis Infectious upper palatal cyst, periodontitis, otitis externa, vulvitis, vaginitis, wound infection and postoperative infection. 3. Deep suppurative diseases: mastitis, lymphadenitis, submandibular gland inflammation, osteomyelitis and osteomyelitis. 4. Acute and chronic bronchitis, asthmatic bronchitis, bronchiectasis, bronchopneumonia, bacterial pneumonia, atypical pneumonia and pulmonary suppuration. 5. Syphilis. 6. Otitis media, paranasal sinusitis and submandibular gland inflammation. 7. Dysentery, enteritis, infectious food poisoning, cholangitis and cholecystitis. 8. Peritonitis. 9. Sepsis and bacteremia. More role
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Common name:
Minocycline hydrochloride capsule
Product No.:
C14200011132
Approval No.:
Gyzz h10960011 (inquired by the State Drug Administration)
Jianke price:
¥69.00
Product specification:
50mg * 10s * 2 plate
Manufacturer:
Wyeth Pharmaceutical Co., Ltd

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        Product name Minocycline hydrochloride capsule (Meiman)
        Main raw materials The main component of this product is minocycline hydrochloride.
        Main role This product is applicable to the following infections caused by pathogens sensitive to this product, such as Staphylococcus, Streptococcus, pneumococcus, Neisseria gonorrhoeae, Shigella, Escherichia coli, Klebsiella, proteus, Pseudomonas aeruginosa, Treponema pallidum and Chlamydia: 1. Urethritis, male nongonococcal urethritis (NGU), prostatitis, gonorrhea, cystitis, epididymitis, intrauterine infection, pyelonephritis, pyelonephritis, pyelonephritis, cystitis, etc. 2. Superficial suppurative infection: acne, tonsillitis, scapulohumeral periarthritis, folliculitis, pyoderma, furuncle, furuncle, carbuncle, cellulitis, sweat gland, sebaceous cyst powder tumor, papillary dermatitis, paronychia, abscess, secondary infection of corns, pharyngitis, dacryocystitis, blepharitis, wheat granuloma, gingivitis, pericoronitis, dental maxillary sinusitis Infectious upper palatal cyst, periodontitis, otitis externa, vulvitis, vaginitis, wound infection and postoperative infection. 3. Deep suppurative diseases: mastitis, lymphadenitis, submandibular gland inflammation, osteomyelitis and osteomyelitis. 4. Acute and chronic bronchitis, asthmatic bronchitis, bronchiectasis, bronchopneumonia, bacterial pneumonia, atypical pneumonia and pulmonary suppuration. 5. Syphilis. 6. Otitis media, paranasal sinusitis and submandibular gland inflammation. 7. Dysentery, enteritis, infectious food poisoning, cholangitis and cholecystitis. 8. Peritonitis. 9. Sepsis and bacteremia.
        Product specification 50mg * 10s * 2 plate
        Usage and dosage Oral. The first dose for adults is 0.2g, and then 0.1g every 12 or 24 hours, or as directed by a doctor. Acne vulgaris 50mg each time, twice a day, 6 weeks as a course of treatment. Patients with renal impairment: for patients with renal impairment, the total daily dose within 24 hours shall not exceed 200mg.
        manufacturing enterprise Wyeth Pharmaceutical Co., Ltd
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        [drug name] Minocycline hydrochloride capsule (Meiman)

        [common name] Minocycline hydrochloride capsule

        [specification and model] 50mg * 10s * 2 plate

        [manufacturer] Wyeth Pharmaceutical Co., Ltd

        [drug type] Western medicine

        [approval No.] Gyzz h10960011

        [validity period] 36 months

        [functional indications] This product is applicable to the following infections caused by pathogens sensitive to this product, such as Staphylococcus, Streptococcus, pneumococcus, Neisseria gonorrhoeae, Shigella, Escherichia coli, Klebsiella, proteus, Pseudomonas aeruginosa, Treponema pallidum and Chlamydia: 1. Urethritis, male nongonococcal urethritis (NGU), prostatitis, gonorrhea, cystitis, epididymitis, intrauterine infection, pyelonephritis, pyelonephritis, pyelonephritis, cystitis, etc. 2. Superficial suppurative infection: acne, tonsillitis, scapulohumeral periarthritis, folliculitis, pyoderma, furuncle, furuncle, carbuncle, cellulitis, sweat gland, sebaceous cyst powder tumor, papillary dermatitis, paronychia, abscess, secondary infection of corns, pharyngitis, dacryocystitis, blepharitis, wheat granuloma, gingivitis, pericoronitis, dental maxillary sinusitis Infectious upper palatal cyst, periodontitis, otitis externa, vulvitis, vaginitis, wound infection and postoperative infection. 3. Deep suppurative diseases: mastitis, lymphadenitis, submandibular gland inflammation, osteomyelitis and osteomyelitis. 4. Acute and chronic bronchitis, asthmatic bronchitis, bronchiectasis, bronchopneumonia, bacterial pneumonia, atypical pneumonia and pulmonary suppuration. 5. Syphilis. 6. Otitis media, paranasal sinusitis and submandibular gland inflammation. 7. Dysentery, enteritis, infectious food poisoning, cholangitis and cholecystitis. 8. Peritonitis. 9. Sepsis and bacteremia.

        [usage and dosage] Oral. The first dose for adults is 0.2g, and then 0.1g every 12 or 24 hours, or as directed by a doctor. Acne vulgaris 50mg each time, twice a day, 6 weeks as a course of treatment. Patients with renal impairment: for patients with renal impairment, the total daily dose within 24 hours shall not exceed 200mg.

        [adverse reactions] According to MedDRA system / organ classification and CIOMS frequency category, the adverse reactions are listed as follows: Common: ≥ 1% Uncommon: ≥ 0.1% and < 1% Rare: ≥ 0.01% and < 0.1% Very rare: < 0.01% Systemic organ classification adverse reactions Abnormal hematolymphatic system Rare: eosinophilia, leucopenia, neutropenia, thrombocytopenia; Very rare: hemolytic anemia, pancytopenia; The incidence is uncertain: agranulocytosis; Cardiovascular abnormalities Very rare: myocarditis, pericarditis; Abnormal ear and labyrinth Rare: hearing impairment and tinnitus; Endocrine system abnormality Very rare: abnormal thyroid function and brown black change of thyroid; Abnormality of gastrointestinal system Rare: diarrhea, nausea, stomatitis, tooth discoloration (including adult tooth discoloration), vomiting; Very rare: dyspepsia, dysphagia, enamel hypoplasia, enterocolitis, esophagitis, esophageal ulcer, glossitis, pancreatitis and pseudomembranous enteritis; Uncertain incidence: oral discoloration (including tongue, lip and gum); Systemic diseases Uncommon: fever; Very rare: discoloration of secretion; Abnormal hepatobiliary system Rare: elevated liver enzymes, hepatitis; Very rare: intrahepatic cholestasis, liver failure (including fatal), hyperbilirubinemia, jaundice; The incidence is uncertain: autoimmune hepatitis; Abnormal immune system Rare: allergic / anaphylactic reactions (including shock), including fatal; Uncertain incidence: hypersensitivity; Infection and infection Very rare: oral and anogenital Candida infection, vulvovaginitis; Metabolic and nutritional abnormalities Rare: anorexia; Abnormalities of muscle, connective tissue and skeletal system Rare: joint pain, lupus like syndrome, myalgia; Very rare: arthritis, bone discoloration, deterioration of systemic lupus erythematosus (SLE), joint stiffness and joint swelling; Nervous system abnormality Common: dizziness (dizziness); Rare: headache, hypoesthesia, paresthesia, brain pseudotumor, vertigo; Very rare: bulging chimney door; Uncertain incidence: convulsion and sedation; Abnormal kidney and urinary system Rare: elevated blood urea nitrogen (BUN); Very rare: acute renal failure, interstitial nephritis; Reproductive system and breast abnormalities Very rare: balanitis; Respiratory, thoracic and mediastinal abnormalities Rare: cough and dyspnea; Very rare: bronchospasm, asthma exacerbation, lung eosinophilia; Uncertain incidence: localized pneumonia; Abnormal skin and subcutaneous tissue Rare: alopecia, pleomorphic erythema, nodular erythema, fixed drug eruption; Excessive skin coloring, photosensitive reaction, itching, rash and urticaria; Very rare: vascular edema, exfoliative dermatitis, excessive nail coloring, Stevens Johnson syndrome, toxic epidermal necrosis, vasculitis; After marketing, thyroid cancer has been reported in patients treated with minocycline, and the causal relationship between minocycline use and thyroid cancer has not been established. The following syndromes have been reported. Deaths have been reported in some cases of these syndromes. Like other serious adverse reactions, if these syndromes occur, the drug should be stopped immediately: ·Allergic reaction syndrome, including epidermal reaction (such as rash or exfoliative dermatitis), eosinophilia and one or more of the following: hepatitis, localized pneumonia, nephritis, myocarditis and pericarditis. Fever and lymphadenopathy may be present. ·Lupus like syndrome, including positive antinuclear antibodies; Joint pain, arthritis, joint stiffness or joint swelling; One or more of the following: fever, myalgia, hepatitis, rash, vasculitis· Serum disease like syndrome, including fever; Urticaria or rash; Joint pain, arthritis, joint stiffness and joint swelling. There may be eosinophilia.

        [precautions] 1. Patients with liver and kidney dysfunction, esophageal passage disorder, the elderly, oral malabsorption or inability to eat, and patients with deterioration of general state (due to vitamin K deficiency). 2. Due to its vestibular toxicity, this product is no longer used as a therapeutic drug for Neisseria meningitidis carriers and Neisseria meningitidis infection. 3. People who are allergic to this product may also be allergic to other tetracyclines. 4. Because it can cause dizziness and burnout, automobile drivers, operators engaged in dangerous machine operation and high-altitude operation should avoid taking this product. 5. When this product is retained in the esophagus and disintegrates, it will cause esophageal ulcer, so you should drink more water, especially before going to bed. 6. Patients with acute Neisseria gonorrhoeae urethritis suspected of primary or secondary syphilis should usually undergo dark field examination. When other types of syphilis are suspected, serological examination should be conducted every month for at least 4 months. 7. The dose of patients with severe renal insufficiency should be lower than the common dose. If long-term treatment is needed, the blood drug concentration should be monitored. 8. Liver and kidney functions should be checked regularly during medication. 9. This product is easy to cause photosensitive dermatitis, so avoid sun exposure after medication. 10. Interference with laboratory test indexes: (1) when measuring the concentration of urinary catecholamine (hingerty method), the measurement results may be high due to the interference of this product on fluorescence. (2) It may increase the measured values of alkaline phosphatase, serum amylase, serum bilirubin and serum aminotransferase (AST, ALT). 11. This product can be taken with food, milk or carbonated beverage. See the inner packaging instructions for details. Please read the instructions carefully and follow the doctor's advice.

        [taboo] It is forbidden to be allergic to any tetracycline or any component of this product.

        [listing Permit Holder] Wyeth Pharmaceutical Co., Ltd

        [packaging unit] box

        [main ingredients] The main component of this product is minocycline hydrochloride.

        [character] The content of this product is yellow to yellowish brown pellets.

        [medication for pregnant and lactating women] 1. This product can enter the fetus through the blood placenta barrier and deposit in the calcium area of teeth and bone, causing fetal enamel dysplasia and inhibiting fetal bone growth; It has teratogenic effect in animal experiments. Therefore, pregnant women and women preparing for pregnancy are prohibited. 2. This product has a high concentration in milk. Although it can form insoluble complex with calcium in milk and has little absorption, it can cause permanent discoloration of teeth, poor enamel development and inhibit the development and growth of infant bones. Therefore, lactating women should stop lactation during medication.

        [medication for children] Because this product can cause permanent discoloration of teeth, poor enamel development and inhibit the development and growth of bones, it is forbidden for children under 8 years old.

        [medication for elderly patients] The clinical trial of this product does not include enough patients over 65 years old, so it is impossible to judge whether the response of the elderly is the same as that of the young. The dose selection of elderly patients should be cautious, usually starting from the minimum dose, because the elderly may have lower liver, kidney or heart function, and may suffer from other diseases or be using other drugs at the same time.

        [storage] Shading, sealed storage.

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          Minocycline hydrochloride capsule (Meiman)

          ¥69.00

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