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Medicine overview

Indications of Chemomycine

Rickettsial Infections

Chemomycine is an established treatment for infections caused by Rickettsia species, including Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox, and tick fevers, when tetracycline-class therapy is appropriate for the patient.

Mycoplasma, Chlamydial and Related Infections

Chemomycine is indicated for respiratory tract infections caused by Mycoplasma pneumoniae, for psittacosis/ornithosis caused by Chlamydophila psittaci, and for infections caused by Chlamydia trachomatis such as lymphogranuloma venereum, trachoma, and inclusion conjunctivitis (uncomplicated urethral, endocervical, or rectal chlamydial infection in adults is preferably treated with other guideline-preferred agents; Chemomycine is an alternative option per susceptibility).

Susceptible Bacterial Infections

Chemomycine is indicated for a range of infections caused by susceptible Gram-positive and Gram-negative organisms, including certain respiratory tract infections, skin and soft-tissue infections, and urinary tract infections, when susceptibility testing supports its use and when more narrow-spectrum agents are unsuitable.

Sexually Transmitted Infections (Alternative Therapy)

Chemomycine is established as an alternative treatment for uncomplicated gonorrhea and for syphilis in patients who are hypersensitive to penicillin, and for chancroid caused by Haemophilus ducreyi, per susceptibility and when first-line agents cannot be used.

Other Established and Adjunct Uses

Chemomycine is used, usually in combination with streptomycin, for brucellosis (combination therapy, not Chemomycine alone, is required for adequate cure); together with an aminoglycoside for tularemia and plague as an alternative agent; as an adjunct to amebicides in intestinal amebiasis; and as an adjunctive, limited-course treatment for inflammatory acne vulgaris in adults, consistent with antibiotic stewardship principles.

Topical/Ophthalmic Use

Topical and ophthalmic formulations containing Chemomycine (often combined with polymyxin B) are used, per local product labeling, for susceptible superficial bacterial infections of the eye (such as bacterial conjunctivitis) and skin; these formulations are dosed and used differently from systemic Chemomycine and are not a substitute for treatment of deep or systemic infection.

Not Indicated For

Chemomycine is not effective against viral infections such as the common cold or influenza, and inappropriate use of Chemomycine for such conditions contributes to antibiotic resistance.

Composition

Each capsule or tablet contains Oxytetracycline (as Oxytetracycline hydrochloride) 250 mg or 500 mg, depending on the marketed strength; injectable and ophthalmic/topical formulations of Oxytetracycline are also available in some markets.

Description

Chemomycine is a broad-spectrum antibiotic belonging to the tetracycline class of medicines, one of the older agents in this class, used to treat a variety of bacterial, rickettsial, and chlamydial infections. Chemomycine works by stopping susceptible bacteria from producing the proteins they need to grow and multiply. Chemomycine is commonly used for rickettsial diseases, certain respiratory and skin infections, as alternative therapy for some sexually transmitted infections, and, in topical/ophthalmic form, for superficial eye and skin infections. Chemomycine does not treat viral infections such as the common cold or flu, and Chemomycine should be taken exactly as prescribed by a qualified healthcare professional.

Therapeutic Class

Antibiotic (Tetracycline-class)

Pharmacology

Oxytetracycline is absorbed from the gastrointestinal tract after oral administration, although absorption of Oxytetracycline is incomplete and is significantly reduced by food, dairy products, and polyvalent cations (calcium, magnesium, iron, aluminum, zinc, bismuth), which chelate Oxytetracycline in the gut. Oxytetracycline is widely distributed in body tissues and fluids, crosses the placenta, and is deposited in growing bone and developing teeth, where it binds to calcium. Oxytetracycline undergoes little to no hepatic metabolism and is excreted mainly unchanged, both in urine (via glomerular filtration) and in bile/feces; unlike some newer tetracyclines, elimination of Oxytetracycline is significantly affected by renal function, so Oxytetracycline tends to accumulate in patients with renal impairment. The elimination half-life of Oxytetracycline is approximately 6 to 10 hours in patients with normal renal function.

Dosage & Administration of Chemomycine

The dose, frequency, and duration of Chemomycine vary by indication, patient age, weight, and renal function, and must be determined by a qualified healthcare professional; the regimen used for one infection is not necessarily appropriate for another. Chemomycine should be taken exactly as prescribed by a physician; do not stop, extend, skip doses, or share this medicine with others without medical advice, even if symptoms improve early, as incomplete courses of Chemomycine promote antibiotic resistance.

Administration of Chemomycine

  • Take Chemomycine on an empty stomach, at least 1 hour before or 2 hours after meals, with a full glass of water, since food and dairy products significantly reduce absorption of Chemomycine.
  • Do not take Chemomycine at the same time as milk, other dairy products, antacids, or calcium, iron, magnesium, or zinc supplements; separate these by at least 2–3 hours from a dose of Chemomycine.
  • Remain sitting or standing (do not lie down) for at least 30–60 minutes after taking Chemomycine to reduce the risk of esophageal irritation or ulceration.
  • Use effective sun protection (sunscreen, protective clothing) and limit prolonged sun/UV exposure, as Chemomycine can increase sensitivity to sunlight.
  • Take Chemomycine exactly as prescribed by your physician; do not stop, extend, skip doses, or share this medicine with others without medical advice.

Interaction of Chemomycine

  • Antacids, dairy products, and calcium, iron, magnesium, or zinc supplements: these form insoluble complexes (chelates) with Chemomycine in the gut, substantially reducing absorption of Chemomycine; separate dosing by several hours.
  • Hormonal (oral) contraceptives: Chemomycine may reduce contraceptive efficacy; advise an additional or backup contraceptive method while taking Chemomycine.
  • Warfarin and other anticoagulants: Chemomycine may potentiate anticoagulant effect by depressing plasma prothrombin activity, requiring closer INR monitoring and possible dose adjustment.
  • Penicillin-class antibiotics: the bacteriostatic action of Chemomycine may antagonize the bactericidal action of penicillins; concurrent use is generally avoided.
  • Digoxin: in a small subset of patients, Chemomycine can increase absorption/levels of digoxin by altering gut flora that normally inactivate it, increasing the risk of digoxin toxicity; monitor if used together.
  • Methoxyflurane and other potentially nephrotoxic drugs: concurrent use with Chemomycine has been associated with fatal nephrotoxicity; avoid combination.
  • Retinoids (e.g., isotretinoin): concurrent use with Chemomycine increases the risk of intracranial hypertension (pseudotumor cerebri); concurrent use should be avoided.

Contraindications

Oxytetracycline is contraindicated in:

  • Patients with known hypersensitivity to Oxytetracycline or to any other tetracycline-class antibiotic.
  • Pregnancy, due to the well-established risk of permanent tooth discoloration and inhibition of bone growth in the developing fetus.
  • Children under 8 years of age for routine use, due to the well-established risk of permanent tooth discoloration (staining, enamel hypoplasia) and effects on bone growth during the period of tooth and bone development.

Side Effects of Chemomycine

Common Side Effects

  • Nausea, vomiting, diarrhea, and abdominal discomfort
  • Loss of appetite
  • Photosensitivity (increased sunburn-type skin reaction)
  • Mild skin rash

Serious Side Effects (Seek Medical Attention)

  • Permanent tooth discoloration or enamel hypoplasia if Chemomycine is used in children under 8 years or during pregnancy — see Contraindications
  • Severe chest pain or pain/difficulty swallowing, which may indicate esophageal irritation or ulceration — take with plenty of water and remain upright (see Precautions and Warnings)
  • Severe headache, blurred or double vision, or vision loss, which may indicate intracranial hypertension (pseudotumor cerebri)
  • Yellowing of the skin or eyes, dark urine, or unusual tiredness, which may indicate liver injury
  • Severe or persistent watery/bloody diarrhea, which may indicate Clostridioides difficile-associated diarrhea or colitis
  • Signs of a severe allergic reaction such as swelling of the face/throat, hives, or difficulty breathing
  • Unusual bruising or bleeding, which may rarely indicate a blood disorder

Pregnancy & Lactation

Pregnancy

Chemomycine is contraindicated in pregnancy. Use of Chemomycine during the second and third trimesters, when fetal teeth and bones are developing, is well established to cause permanent discoloration of the teeth (yellow-gray-brown staining) and enamel hypoplasia, and may inhibit fetal bone growth. Because of this well-documented, class-wide risk, Chemomycine should not be used in pregnant women; a physician should be consulted so that an alternative antibiotic can be selected. Any inadvertent exposure to Chemomycine during pregnancy should be discussed promptly with a physician.

Breastfeeding

Chemomycine passes into breast milk. Because of the risk of tooth discoloration and effects on bone growth in the nursing infant, Chemomycine should be avoided during breastfeeding; a physician should be consulted so that an alternative antibiotic considered safer in lactation can be used if antibiotic therapy is required.

Precautions & Warnings

  • Tooth discoloration and bone growth effects (children and pregnancy): Chemomycine, like other tetracyclines, causes permanent tooth discoloration and enamel hypoplasia when used during tooth development (second half of pregnancy, infancy, and childhood up to about 8 years), and may inhibit bone growth in the fetus and young children; this is a well-established, class-wide effect and is the basis for the contraindication in pregnancy and in children under 8 years — see Contraindications.
  • Photosensitivity: Chemomycine can cause an exaggerated sunburn-like skin reaction; use sun protection and limit sun/UV exposure while taking Chemomycine.
  • Esophageal irritation and ulceration: take Chemomycine with plenty of water, remain upright afterward, and avoid bedtime dosing.
  • Hepatotoxicity: rare but serious liver injury (including fatty liver/hepatic failure) has been reported with Chemomycine, particularly with high doses, intravenous administration, pregnancy, or pre-existing renal or hepatic impairment; use with caution and monitor liver function in at-risk patients.
  • Renal impairment: Chemomycine accumulates in patients with reduced kidney function and can increase azotemia and worsen renal impairment; Chemomycine should be used with caution, at reduced frequency, and with monitoring of renal function in such patients, or an alternative antibiotic should be considered.
  • Intracranial hypertension (pseudotumor cerebri): tetracycline-class drugs including Chemomycine have been associated with raised intracranial pressure, more often in women of childbearing age; symptoms include severe headache and visual disturbance. Discontinue Chemomycine promptly if this occurs.
  • Superinfection: prolonged use of Chemomycine may lead to overgrowth of non-susceptible organisms, including fungal infections and C. difficile-associated diarrhea; report new symptoms to a healthcare professional.
  • Antibiotic stewardship: take Chemomycine exactly as prescribed by your physician; do not stop, extend, skip doses, or share this medicine with others without medical advice, as inappropriate use of Chemomycine promotes antibiotic resistance.
  • Not effective against viral infections: Chemomycine treats bacterial infections only and has no effect on viruses such as those causing the common cold or influenza.

Overdose Effects of Chemomycine

Reported effects of Chemomycine overdose are generally an extension of its known side effects, particularly gastrointestinal upset (nausea, vomiting, diarrhea) and esophageal or gastric irritation. No specific antidote for Chemomycine overdose exists. If an overdose of Chemomycine is suspected, seek immediate medical attention or contact emergency services or a poison control center right away; do not attempt specific home treatment. Management of Chemomycine overdose is generally supportive and symptomatic, guided by a physician; Chemomycine is not significantly removed by hemodialysis.

Storage Conditions

Store at room temperature (below 30°C), away from light and moisture. Keep out of reach of children.

Use In Special Populations

Children

Chemomycine is contraindicated in children under 8 years of age for routine use, due to the well-established risk of permanent tooth discoloration, enamel hypoplasia, and effects on bone growth (see Contraindications). In children over 8 years, Chemomycine may be used when clearly indicated, at a weight-based dose of 15–25 mg/kg/day in divided doses, not exceeding the usual adult dose.

Elderly

No specific dose adjustment of Chemomycine is established for older adults on the basis of age alone, but renal function should be assessed before and during treatment, since Chemomycine accumulates in renal impairment, which is more common in this age group.

Renal Impairment

Chemomycine is eliminated substantially by the kidneys and accumulates in patients with reduced renal function, which can worsen azotemia and increase the risk of toxicity; Chemomycine should be used with caution, at a reduced dosing frequency, and with monitoring of renal function, or an alternative antibiotic not dependent on renal clearance should be considered in significant renal impairment.

Hepatic Impairment

Chemomycine should be used with caution in patients with hepatic impairment, since tetracyclines including Chemomycine have been associated with hepatotoxicity, particularly at higher doses; dose reduction and liver function monitoring are advised.

Pregnant and Breastfeeding Women

See the Pregnancy and Lactation section above; Chemomycine is contraindicated in pregnancy and should be avoided during breastfeeding.

Duration Of Treatment

The duration of treatment with Chemomycine is set by the prescriber and depends on the indication: commonly 7–14 days for uncomplicated bacterial and rickettsial infections (continuing at least 24–48 hours after fever resolves for rickettsial disease), 3 weeks in combination therapy for brucellosis, and 15–30 days as alternative therapy for syphilis depending on stage. For acne, courses of Chemomycine are typically limited and periodically reassessed rather than continued indefinitely, consistent with antibiotic stewardship. Patients should take Chemomycine for exactly as long as prescribed and should not stop, extend, skip doses, or repeat a course without medical advice.

Drug Classes

Tetracycline-class antibiotic

Mode Of Action

Oxytetracycline is a bacteriostatic antibiotic. Oxytetracycline binds reversibly to the 30S ribosomal subunit of susceptible bacteria, blocking the binding of aminoacyl-tRNA to the mRNA-ribosome complex. This prevents addition of amino acids to the growing peptide chain, inhibiting bacterial protein synthesis and thereby arresting bacterial growth and multiplication without directly killing the organism. Oxytetracycline is active against a broad range of Gram-positive and Gram-negative bacteria as well as rickettsiae, mycoplasma, and chlamydiae.

Pregnancy

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Pediatric Uses

Chemomycine is contraindicated in children under 8 years of age for routine use because of the well-established risk of permanent tooth discoloration, enamel hypoplasia, and inhibition of bone growth that occurs when tetracyclines are used during the period of tooth and bone development. In children over 8 years, when a tetracycline is clearly indicated and no suitable alternative exists, Chemomycine may be dosed at 15–25 mg/kg/day in equally divided doses every 6 hours, not exceeding the usual adult dose. Safety and efficacy of Chemomycine in neonates and infants have not been established, and use in this age group is not recommended outside exceptional, physician-directed circumstances. Any pediatric use of Chemomycine should be guided by a pediatrician weighing the specific indication, the child's age, and the availability of alternative antibiotics.

Frequently Asked Questions

Q: What is Chemomycine 250 mg Capsule used for?

A: Chemomycine 250 mg Capsule is a tetracycline-class antibiotic used to treat a range of bacterial and rickettsial infections, including Rocky Mountain spotted fever and other rickettsial diseases, certain respiratory and skin infections, and, as alternative therapy, some sexually transmitted infections such as syphilis and gonorrhea in penicillin-allergic patients. Topical/ophthalmic forms of Chemomycine 250 mg Capsule are used for superficial eye and skin infections. Chemomycine 250 mg Capsule does not treat viral infections.

Q: What is the usual dosage of Chemomycine 250 mg Capsule?

A: Adult dosing of Chemomycine 250 mg Capsule commonly ranges from 250 mg once daily to 250–500 mg every 6 hours, depending on the infection being treated, with some indications such as brucellosis requiring combination therapy and a longer course. There is no single dose of Chemomycine 250 mg Capsule that applies to every condition; only a qualified healthcare professional can determine the correct dose for a given patient.

Q: Can Chemomycine 250 mg Capsule be taken with milk or antacids?

A: No. Milk, other dairy products, antacids, and supplements containing calcium, iron, magnesium, or zinc bind to Chemomycine 250 mg Capsule in the gut and substantially reduce how much is absorbed. Chemomycine 250 mg Capsule should be taken on an empty stomach, at least 1 hour before or 2 hours after meals and dairy, and separated by at least 2–3 hours from these products.

Q: Is Chemomycine 250 mg Capsule safe during pregnancy?

A: No. Chemomycine 250 mg Capsule is contraindicated during pregnancy because it is well established to cause permanent discoloration of the developing baby's teeth and can inhibit fetal bone growth, particularly with use in the second and third trimesters. Pregnant women should not take Chemomycine 250 mg Capsule; a physician should be consulted so that a safer alternative antibiotic can be prescribed.

Q: Can children take Chemomycine 250 mg Capsule?

A: Chemomycine 250 mg Capsule is contraindicated in children under 8 years of age because it is well established to cause permanent staining of the teeth and enamel hypoplasia, and can affect bone growth, during the period when teeth and bones are developing. In children over 8 years, Chemomycine 250 mg Capsule may be used when clearly needed, at a weight-based dose determined by a doctor.

Q: What medicines interact with Chemomycine 250 mg Capsule?

A: Chemomycine 250 mg Capsule interacts with antacids, dairy products, and calcium, iron, magnesium, or zinc supplements (all reduce absorption of Chemomycine 250 mg Capsule), warfarin and other anticoagulants (increased bleeding risk), penicillin-type antibiotics (reduced effectiveness of the penicillin), hormonal oral contraceptives (possible reduced contraceptive effect), digoxin (possible increased digoxin levels in some patients), and retinoids such as isotretinoin (increased risk of raised pressure around the brain). Tell your doctor or pharmacist about all medicines you take before starting Chemomycine 250 mg Capsule.

Disclaimer

The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.

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