The manufacturer recommended dosage is 10—20 mg/kg/day PO, given in 1—2 divided doses, not to exceed 1000 mg/day. You can mix your dose with a little water if needed.If your acid problems persist or worsen after you have used this product for 1 week, or if you think you have a serious medical problem, seek immediate medical attention. This website also contains material copyrighted by 3rd parties. Usual daily dose: 500 mg PO q12hr or 250 mg PO q6hr (ie, 1000 mg/day)Higher doses (eg, 500 mg PO q6hr) may be required for severe infections or for those infections which do not respond to the smaller dosesRecommended initial dosage: 1 g/day PO in divided doses (based on the judgement of the clinician)When improvement is noted, gradually reduce dose to maintenance levels ranging from 125-500 mg/daySome patients may be able to maintain adequate remission of lesions with alternate day or intermittent therapyDuration of long-term treatment which can safely be recommended has not been established500 mg PO q6hr for 3 weeks accompanied by streptomycin, 1 g IM BID for the first week, THEN qDay the second weekInfections in adults caused by Chlamydia trachomatisUpper respiratory tract infections caused by Streptococcus pyogenes, Streptococcus pneumoniae and Haemophilus influenzae; tetracycline should not be used for streptococcal disease unless the organism has been demonstrated to be susceptibleLower respiratory tract infections caused by Streptococcus pyogenes, Streptococcus pneumoniae, Mycoplasma pneumoniae (Eaton agent, and Klebsiella spp)Skin and soft tissue infections caused by Streptococcus pyogenes, Staphylococcus aureus; tetracyclines are not the drugs of choice in the treatment of any type of staphylococcal infectionsInfections caused by rickettsia including Rocky Mountain spotted fever, typhus group infections, Q fever, rickettsialpoxInfections caused by Chlamydia trachomatis (eg, uncomplicated urethral, endocervical or rectal infections, inclusion conjunctivitis, trachoma, and lymphogranuloma venereum)Granuloma inguinale caused by Klebsiella granulomatis Relapsing fever caused by Borrelia spp Bartonellosis caused by Bartonella bacilliformisBrucellosis caused by Brucella species (tetracycline may be used in conjunction with an aminoglycoside)As adjunctive therapy in intestinal amebiasis caused by Entamoeba histolyticaUrinary tract infections caused by susceptible strains (eg, Escherichia coli, Klebsiella)Other infections caused by susceptible gram-negative organisms such as E coli, Enterobacter aerogenes, Shigella spp, Acinetobacter spp, Klebsiella spp, and Bacteroides sppIn severe acne, adjunctive therapy with tetracycline may be usefulSyphilis and yaws caused by Treponema pallidum and pertenue, respectivelyVincent’s infection caused by Fusobacterium fusiformeAnthrax caused by Bacillus anthracis Infections due to Listeria monocytogenesIn the treatment of streptococcal infections, administered for at least 10 daysAs with other antibacterials, use of this drug may result in overgrowth of nonsusceptible organisms, including fungiIf superinfection occurs, discontinue antibacterial and institute appropriate therapyTreat all infections due to Group A beta-hemolytic streptococci for at least 10 daysPerform incision and drainage or other surgical procedures in conjunction with antibacterial therapy, when indicatedPrescribing tetracycline in the absence of proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria≤8 years: Not recommended; tooth discoloration and enamel hypoplasia may occur with use in young children>8 years: 25-50 mg/kg/day PO divided q6hr; not to exceed 3 g/day Gastrointestinal: anorexia, nausea, epigastric distress, vomiting, diarrhea, glossitis, esophagitis, esophageal ulceration, black hairy tongue, dysphagia, enterocolitis, and inflammatory lesions (with Candida overgrowth) in the anogenital regionTeeth: Permanent discoloration of teeth, enamel hypoplasiaSkin: Maculopapular and erythematous rashes, exfoliative dermatitis, onycholysis and discoloration of the nails, photosensitivityHypersensitivity reactions: Urticaria, angioneurotic edema, anaphylaxis, anaphylactoid purpura, pericarditis, exacerbation of systemic lupus erythematosus, and serum sickness-like reactions, as fever, rash, and arthralgiaBlood: Hemolytic anemia, thrombocytopenia, thrombocytopenic purpura, neutropenia and eosinophilia have been reportedPhotosensitivity may occur with prolonged exposure to sunlight or tanning equipmentConsider drug serum level determinations in prolonged therapyTetracycline use during tooth development (last half of pregnancy through age 8 years) can cause permanent discoloration of teethAntianabolic action of the tetracyclines may cause an increase in BUN; in patients with significantly impaired renal function, higher serum levels of tetracycline may lead to azotemia, hyperphosphatemia and acidosisFanconi-like syndrome may occur with outdated tetracyclinesIntracranial hypertension (IH, pseudotumor cerebri) has been associated with the use of tetracyclines; although IH typically resolve after discontinuing treatment, the possibility for permanent visual loss exists; if visual disturbance occurs during treatment, prompt ophthalmologic evaluation is warrantedAll tetracyclines form a stable calcium complex in any bone forming tissue; decrease in fibula growth rate has been observed in premature infants given oral tetracycline in doses of 25 mg/kg q6hr; reaction was shown to be reversible when discontinuing drugAvoid 1st trimester; contraindicated 2nd and 3rd trimestersPregnant women with renal disease may be more prone to develop tetracycline-associated liver failureThe effect of tetracyclines on labor and delivery is unknownShort-term use of tetracycline is acceptable in nursing mothersA number of reviews have stated that tetracycline is contraindicated during breastfeeding because of possible staining of infants' dental enamel or bone deposition of tetracyclines; however, a close examination of available literature indicates that there is not likely to be harm in short-term use of tetracycline during lactation because milk levels are low and absorption by the infant is inhibited by the calcium in breast milkTetracycline is excreted into breast milk in low concentrations (milk:plasma ratio ranges between 0.25 and 1.5)NIH LactMed and the American Academy of Pediatrics classifies tetracycline as compatible with breastfeedingA: Generally acceptable.
Be sure to check with your pharmacist before taking antacids with any other If someone has overdosed and has serious symptoms such as passing out or Keep all regular medical and laboratory appointments.Lifestyle changes such as stress reduction programs, stopping If you are taking this product on a regular schedule and miss a dose, take it as soon as you remember.
Take your next dose at the regular time.
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