Minocycline (Systemic)
Drug class: Antineoplastic Agents
Usage of Minocycline (Systemic)
Respiratory Tract Infections
Treatment of respiratory tract infections caused by Mycoplasma pneumoniae.
Treatment of respiratory tract infections caused by Haemophilus influenzae, Streptococcus pneumoniae, or Klebsiella. Should only be used for treatment of infections caused by these bacteria when in vitro susceptibility tests indicate the organism is susceptible.
Acinetobacter Infections
Alternative to imipenem or meropenem for treatment of infections caused by Acinetobacter.
Acne
Adjunctive treatment of moderate to severe inflammatory acne. Not indicated for treatment of noninflammatory acne.
Actinomycosis
Treatment of actinomycosis caused by Actinomyces israelii; oral tetracyclines (usually doxycycline or tetracycline) used as follow-up after initial parenteral penicillin G.
Amebiasis
Adjunct to amebicides for treatment of acute intestinal amebiasis. Tetracyclines not included in current recommendations for treatment of amebiasis caused by Entamoeba.
Anthrax
Alternative to doxycycline for postexposure prophylaxis to reduce the incidence or progression of disease following a suspected or confirmed exposure to aerosolized Bacillus anthracis spores (inhalational anthrax). Initial drug of choice for such prophylaxis is ciprofloxacin or doxycycline; doxycycline is the preferred tetracycline because of ease of administration and proven efficacy in monkey studies.
Alternative to doxycycline for treatment of inhalational anthrax when a parenteral regimen is not available (e.g., supply or logistic problems because large numbers of individuals require treatment in a mass casualty setting). A multiple-drug parenteral regimen (ciprofloxacin or doxycycline and 1 or 2 other anti-infectives predicted to be effective) is preferred for treatment of inhalational anthrax that occurs as the result of exposure to anthrax spores in the context of biologic warfare or bioterrorism.
Bartonella Infections
Treatment of bartonellosis caused by Bartonella bacilliformis.
Brucellosis
Treatment of brucellosis; tetracyclines (usually doxycycline or tetracycline) considered drugs of choice. Tetracyclines used in conjunction with other anti-infectives (e.g., streptomycin or gentamicin and/or rifampin), especially for severe infections or when there are complications (e.g., endocarditis, meningitis, osteomyelitis).
Campylobacter Infections
Treatment of infections caused by Campylobacter. Tetracyclines (usually doxycycline) are alternatives, not drugs of choice for C. jejuni.
Chancroid
Treatment of chancroid caused by Haemophilus ducreyi. Not included in CDC recommendations for treatment of chancroid.
Chlamydial Infections
Treatment of uncomplicated urethral, endocervical, or rectal infections caused by Chlamydia trachomatis. Doxycycline is the preferred tetracycline for treatment of these infections, including presumptive treatment of chlamydial infections in patients with gonorrhea.
Treatment of trachoma and inclusion conjunctivitis caused by C. trachomatis. Consider that anti-infectives may not eliminate C. trachomatis in all cases of chronic trachoma.
Treatment of lymphogranuloma venereum (genital, inguinal, or anorectal infections) caused by C. trachomatis. Doxycycline is the preferred tetracycline for these infections.
Treatment of psittacosis (ornithosis) caused by C. psittaci. Doxycycline and tetracycline are drugs of choice. For initial treatment of severely ill patients, use IV doxycycline.
Clostridium Infections
Alternative for treatment of infections caused by Clostridium. Tetracyclines are alternatives to metronidazole or penicillin G for adjunctive treatment of C. tetani infections.
Enterobacteriaceae Infections
Treatment of infections caused by susceptible Escherichia coli, Enterobacter aerogenes, Klebsiella, or Shigella. Should only be used for treatment of infections caused by these common gram-negative bacteria when other appropriate anti-infectives are contraindicated or ineffective and when in vitro susceptibility tests indicate the organism is susceptible.
Fusobacterium Infections
Alternative to penicillin G for treatment of infections caused by Fusobacterium fusiforme (Vincent’s infection).
Gonorrhea and Associated Infections
Alternative for treatment of uncomplicated gonorrhea (including urethritis) caused by susceptible Neisseria gonorrhoeae. Tetracyclines are considered inadequate therapy and are not recommended by CDC for treatment of gonorrhea.
Granuloma Inguinale (Donovanosis)
Treatment of granuloma inguinale (donovanosis) caused by Calymmatobacterium granulomatis. Doxycycline is the tetracycline recommended as drug of choice by CDC.
Listeria Infections
Alternative for treatment of listeriosis caused by Listeria monocytogenes. Not usually considered a drug of choice or alternative for these infections.
Malaria
Other tetracyclines (doxycycline) used for prevention of malaria; data insufficient to evaluate efficacy of minocycline for malaria prevention. CDC recommends that individuals receiving long-term minocycline therapy (e.g., for acne) who also require doxycycline malaria prophylaxis should discontinue minocycline 1–2 days prior to travel and initiate doxycycline for such prophylaxis; minocycline can be reinitiated after doxycycline malaria prophylaxis is finished.
Mycobacterial Infections
Alternative for use in multiple-drug regimens for treatment of multibacillary leprosy† [off-label]. WHO recommends minocycline as an alternative for multibacillary leprosy regimens in patients who will not accept or cannot tolerate clofazimine and when rifampin cannot be used because of adverse effects, intercurrent disease (e.g., chronic hepatitis), or infection with rifampin-resistant Mycobacterium leprae.
Component of a single-dose rifampin-based multiple-drug regimen (ROM) for treatment of single-lesion paucibacillary leprosy† [off-label] (i.e., a single skin lesion with definite loss of sensation but without nerve trunk involvement). A ROM regimen of a single dose of rifampin, single dose of ofloxacin, and single dose of minocycline is recommended by WHO as an acceptable and cost-effective alternative regimen in antileprosy programs that have detected a large number of patients (e.g., more than 1000 annually) with single-lesion paucibacillary leprosy.
Treatment of cutaneous infections caused by M. marinum; a drug of choice.
Neisseria meningitidis Infections
Elimination of nasopharyngeal carriage of Neisseria meningitidis. CDC and AAP recommend use of rifampin, ceftriaxone, or ciprofloxacin for such carriers and no longer recommend use of minocycline.
Should not be used for treatment of infections caused by N. meningitidis.
Nocardiosis
Tetracyclines are alternative to co-trimoxazole for treatment of nocardiosis† [off-label] caused by Nocardia.
Nongonococcal Urethritis
Treatment of nongonococcal urethritis (NGU) caused by Ureaplasma urealyticum, C. trachomatis, or Mycoplasma. Doxycycline usually is the tetracycline of choice for NGU.
Consider that some cases of recurrent urethritis following treatment may be caused by tetracycline-resistant U. urealyticum.
Plague
Treatment of plague caused by Yersinia pestis. Regimen of choice is streptomycin or gentamicin; alternatives are doxycycline, tetracycline, ciprofloxacin, or chloramphenicol.
Relapsing Fever
Treatment of relapsing fever caused by Borrelia recurrentis. Tetracyclines are drugs of choice.
Rheumatoid Arthritis
Treatment of rheumatoid arthritis† [off-label]. One of several disease-modifying antirheumatic drugs (DMARDs) that can be used when DMARD therapy is appropriate.
Rickettsial Infections
Treatment of rickettsial infections including Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox, and tick fevers caused by Rickettsiae. Doxycycline is the drug of choice for most rickettsial infections.
Stenotrophomonas maltophilia Infections
Treatment of infections caused by Stenotrophomonas maltophilia† [off-label]. Alternative to co-trimoxazole.
Syphilis
Alternative to penicillin G for treatment of primary, secondary, latent, or tertiary syphilis (not neurosyphilis) in nonpregnant adults and adolescents hypersensitive to penicillins. Doxycycline and tetracycline are the preferred tetracyclines in patients hypersensitive to penicillins. Use tetracyclines only if compliance and follow-up can be ensured since efficacy not well documented.
Tularemia
Treatment of tularemia caused by Francisella tularensis. Tetracyclines (usually doxycycline) considered alternatives to streptomycin (or gentamicin); risk of relapse and primary treatment failure may be higher than with aminoglycosides.
Vibrio Infections
Treatment of cholera caused by Vibrio cholerae. Doxycycline and tetracycline are drugs of choice; used as an adjunct to fluid and electrolyte replacement in moderate to severe disease.
Yaws
Alternative to penicillin G for treatment of yaws caused by Treponema pertenue.
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How to use Minocycline (Systemic)
Administration
Administer orally. Has been administered by IV infusion, but parenteral preparations no longer available in US.
Oral Administration
Tablets and pellet-filled capsules should be administered at least 1 hour before or 2 hours after meals. Capsules may be administered with or without food.
Administer capsules, pellet-filled capsules, and tablets with adequate amounts of fluid to reduce the risk of esophageal irritation and ulceration.
The pellet-filled capsules should be swallowed whole.
Dosage
Available as minocycline hydrochloride; dosage expressed in terms of minocycline.
Pediatric Patients
General Pediatric Dosage OralChildren >8 years of age: 4 mg/kg initially followed by 2 mg/kg every 12 hours.
Mycobacterial Infections Leprosy† OralChildren 5–14 years of age: for treatment of single-lesion paucibacillary leprosy† in certain patient groups, WHO recommends a single-dose ROM regimen that includes a single 300-mg dose of rifampin, a single 200-mg dose of ofloxacin, and a single 50-mg dose of minocycline.
Children <5 years of age: WHO recommends that an appropriately adjusted dose of each drug in the single-dose ROM regimen be used.
Adults
General Adult Dosage Oral200 mg initially followed by 100 mg every 12 hours.
Alternatively, if more frequent doses are preferred, 100–200 mg initially followed by 50 mg 4 times daily.
Acne Oral50 mg 1–3 times daily.
Chlamydial Infections Uncomplicated Urethral, Endocervical, or Rectal Infections Oral100 mg every 12 hours given for ≥7 days.
Gonorrhea and Associated Infections Uncomplicated Gonorrhea (except Urethritis or Anorectal in Men) Oral200 mg initially followed by 100 mg every 12 hours given for ≥ 4 days; follow-up cultures should be done within 2–3 days after completion of therapy.
No longer recommended for gonorrhea by CDC or other experts.
Gonococcal Urethritis in Men Oral100 mg every 12 hours given for 5 days.
No longer recommended for gonorrhea by CDC or other experts.
Mycobacterial Infections Leprosy† OralFor treatment of multibacillary leprosy† in those who cannot receive rifampin because of adverse effects, intercurrent disease (e.g., chronic hepatitis), or infection with rifampin-resistant M. leprae, WHO recommends supervised administration of a regimen of clofazimine (50 mg daily), ofloxacin (400 mg daily), and minocycline (100 mg daily) given for 6 months, followed by a regimen of clofazimine (50 mg daily) and minocycline (100 mg daily) given for at least an additional 18 months.
For treatment of multibacillary leprosy in adults who will not accept or cannot tolerate clofazimine, WHO recommends supervised administration of a once-monthly ROM regimen that includes rifampin (600 mg once monthly), ofloxacin (400 mg once monthly), and minocycline (100 mg once monthly) given for 24 months.
For treatment of single-lesion paucibacillary leprosy† in certain patient groups, WHO recommends a single-dose ROM regimen that includes a single 600-mg dose of rifampin, a single 400-mg dose of ofloxacin, and a single 100-mg dose of minocycline.
Mycobacterium marinum Infections OralManufacturers state optimum dosage has not been established, but 100 mg every 12 hours for 6–8 weeks has been effective.
100 mg twice daily for ≥3 months recommended by ATS for treatment of cutaneous infections. A minimum of 4–6 weeks of treatment usually is necessary to determine whether the infection is responding.
Neisseria meningitidis Infections N. meningitidis Carriers Oral100 mg every 12 hours given for 5 days.
Nocardiosis† Oral200 mg initially followed by 100 mg every 12 hours given for 12–18 months.
Nongonoccocal Urethritis Oral100 mg every 12 hours given for ≥ 7 days.
Rheumatoid Arthritis† Oral100 mg twice daily. A benefit may be evident within 1–3 months.
Syphilis Oral200 mg initially followed by 100 mg every 12 hours given for 10–15 days. Close follow-up and laboratory tests are recommended.
Vibrio Infections Cholera Oral200 mg initially followed by 100 mg every 12 hours given for 2–3 days.
Prescribing Limits
Pediatric Patients
OralDo not exceed usual adult dosage.
Special Populations
Renal Impairment
Data insufficient to make recommendations regarding dosage adjustment. Dosage should not exceed 200 mg daily in patients with impaired renal function.
Warnings
Contraindications
Warnings/Precautions
Warnings
Dental and Bone EffectsUse during tooth development (e.g., pregnancy, children <8 years of age) may cause permanent yellow-gray to brown discoloration of teeth and enamel hypoplasia. Effects are most common following long-term use, but may occur following repeated short-term use.
Tetracyclines form a stable calcium complex in any bone-forming tissue. Reversible decrease in fibula growth rate has occurred in prematures receiving tetracycline.
Use not recommended in children <8 years of age unless other appropriate drugs are ineffective or are contraindicated or unless the benefits in certain indications (e.g., anthrax) outweigh the risks. (See Pediatric Use under Cautions.)
Fetal/Neonatal MorbidityAnimal studies indicate possible fetal toxicity (e.g., retardation of skeletal development) and embryotoxicity. If used during pregnancy or if patient becomes pregnant while receiving minocycline, patient should be apprised of the potential hazard to the fetus. (See Pregnancy under Cautions.)
Nervous System EffectsPossiblility of adverse CNS effects (light-headedness, dizziness, vertigo) that may impair ability to drive vehicles or operate hazardous machinery. Vestibular reactions occur more frequently with minocycline than with other tetracyclines. Symptoms may disappear during therapy and usually rapidly disappear when the drug is discontinued.
Benign intracranial hypertension (pseudotumor cerebri) in adults reported with tetracyclines; usually manifested as headache and blurred vision. Bulging fontanels reported in infants. Effects usually resolve when drug discontinued, but possibility for permanent sequelae exists.
Renal EffectsTetracyclines have antianabolic effects and may increase BUN.
In patients with impaired renal function, high serum minocycline concentrations may result in azotemia, hyperphosphatemia, and acidosis. Excessive drug accumulation and possible liver toxicity may occur if usual dosage is used in patients with renal impairment. (See Renal Impairment under Dosage and Administration.)
Laboratory MonitoringPeriodically assess organ system function, including renal, hepatic and hematopoietic, during long-term therapy.
Sensitivity Reactions
Photosensitivity ReactionsPhotosensitivity, manifested by an exaggerated sunburn reaction, reported with tetracyclines.
Photosensitivity reactions may develop within a few minutes to several hours after sun exposure and usually persist 1–2 days after discontinuance of the drug. Most reactions result from accumulation of tetracyclines in skin and are phototoxic in nature; photoallergic reactions may also occur.
Discontinue drug at first evidence of skin erythema.
Hypersensitivity ReactionsUrticaria, angioneurotic edema, polyarthralgia, anaphylaxis, anaphylactoid purpura, pericarditis, exacerbation of systemic lupus erythematosus and, rarely, pulmonary infiltrates with eosinophilia have been reported. A transient lupus-like syndrome and serum sickness-like reaction also have been reported.
General Precautions
HepatotoxicityHepatotoxicity has been reported. Use with caution in patients with hepatic dysfunction and in those receiving other hepatotoxic drug.
SuperinfectionPossible emergence and overgrowth of nonsusceptible bacteria or fungi. Discontinue drug and institute appropriate therapy if superinfection occurs.
Selection and Use of Anti-infectivesTo reduce development of drug-resistant bacteria and maintain effectiveness of minocycline and other antibacterials, use only for treatment or prevention of infections proven or strongly suspected to be caused by susceptible bacteria.
When selecting or modifying anti-infective therapy, use results of culture and in vitro susceptibility testing. In the absence of such data, consider local epidemiology and susceptibility patterns when selecting anti-infectives for empiric therapy.
Because many strains of Acinetobacter, Bacteroides, Enterobacter, E. coli, Klebsiella, Shigella, S. pyogenes (group A β-hemolytic streptococci), S. pneumoniae, enterococci, and α-hemolytic streptococci are resistant to tetracyclines (including minocycline), in vitro susceptibility tests should be performed if the drug is used for treatment of infections caused by these bacteria.
Incision and drainage or other surgical procedures should be performed in conjunction with minocycline therapy when indicated.
Specific Populations
PregnancyCategory D. (See Fetal/Neonatal Morbidity under Cautions.)
Should not be used in pregnant women unless, in the judgment of the clinician, it is essential for the welfare of the patient and benefits outweigh the risks. CDC and others state tetracyclines can be used when necessary for treatment of inhalational anthrax in pregnant women. Since adverse effects on developing teeth and bones are dose-related, CDC suggests the tetracyclines might be used for a short period (7–14 days) before 6 months of gestation; some clinicians recommend periodic liver function testing if used in pregnant women.
LactationDistributed into milk; discontinue nursing or the drug.
AAP states maternal use of tetracyclines usually is compatible with breast-feeding since absorption of the drugs by nursing infants is negligible.
Pediatric UseShould not be used in children <8 years of age unless benefits outweigh the risks. (See Dental and Bone Effects under Cautions.)
Geriatric UseInsufficient experience in those ≥65 years of age to determine whether they respond differently than younger adults.
Select dosage with caution because of age-related decreases in hepatic, renal, and/or cardiac function and concomitant disease and drug therapy; generally initiate therapy using the low end of the dosing range.
Hepatic ImpairmentUse with caution.
Renal ImpairmentMay result in high serum minocycline concentrations and azotemia, hyperphosphatemia, and acidosis.
Excessive drug accumulation and possible liver toxicity may occur if usual dosage is used in patients with renal impairment. Dosage adjustment necessary in patients with impaired renal function. (See Renal Impairment under Dosage and Administration.)
Monitor serum creatinine and BUN.
Because usual dosage of doxycycline can be used in patients with impaired renal function, it may be preferred when a tetracycline is indicated in a patient with impaired renal function.
Common Adverse Effects
GI effects (anorexia, nausea, vomiting, diarrhea); CNS effects (dizziness, vertigo); hypersensitivity reactions; dose-related BUN increases.
What other drugs will affect Minocycline (Systemic)
Specific Drugs
Drug
Interaction
Comments
Antacids (aluminum-, calcium-, or magnesium-containing)
Decreased minocycline absorption
Administer antacids containing aluminum, calcium, or magnesium 1–2 hours before or after minocycline
Anticoagulants, oral
Possible increased anticoagulant effect; tetracyclines may impair utilization of prothrombin or decrease vitamin K production by intestinal bacteria
Monitor PT carefully; adjust anticoagulant dosage as needed
Ergot Alkaloids
Increased risk of ergotism
Hormonal contraceptives
Possible decreased effectiveness of oral contraceptives
Use alternative nonhormonal contraceptives
Iron-containing preparations
Possible decreased absorption of minocycline
Administer minocycline 2 hours before or 3 hours after an oral iron preparation
Isotretinoin
Possible additive adverse nervous system effects; both minocycline and isotretinoin have been associated with pseudotumor cerebri
Avoid use of isotretinoin shortly before, during, or after minocycline therapy
Methoxyflurane
Possible fatal nephrotoxicity
Concomitant use not recommended
Penicillins
Possible antagonism
Concomitant use not recommended
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