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Authoritative Clinical Reference
| Form | Strengths |
|---|---|
| Capsules | 100 mg |
| Tablets | 100 mg |
| Dispersible tablets | 100 mg |
| Tablets (extended-release) | 40 mg (sub-antimicrobial dose for rosacea) |
| Injection (powder for reconstitution) | 100 mg/vial |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7 days (extend to 14 days if severe or delayed response) |
| Clinical notes | First-line therapy per ICMR/NCDC guidelines; continue until afebrile for 48–72 hours; highly endemic in Himalayan foothills, NE India, South India |
| Parameter | Recommendation |
|---|---|
| Starting dose | 300 mg single dose OR 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily if multi-dose regimen |
| Maximum dose | 300 mg/day |
| Duration | Single dose or 3 days |
| Clinical notes | Adjunct to ORS; reduces stool output and vibrio shedding; per NCDC outbreak guidelines |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7 days |
| Clinical notes | First-line per NACO STI guidelines; treat partner simultaneously; test-of-cure not routinely needed |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7 days |
| Clinical notes | Covers Chlamydia and Mycoplasma genitalium; combine with ceftriaxone if gonorrhoea not excluded |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 14 days |
| Clinical notes | Use with ceftriaxone 250 mg IM single dose ± metronidazole 500 mg twice daily; per NACO syndromic management guidelines |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7 days |
| Clinical notes | Effective if started within first 4 days of illness; IV penicillin preferred for severe/icteric disease |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 6 weeks |
| Clinical notes | Always combine with streptomycin (first 2–3 weeks) OR rifampicin (full 6 weeks); monotherapy leads to high relapse |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg once daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg once daily |
| Maximum dose | 100 mg/day |
| Duration | Start 1–2 days before travel; continue during stay + 4 weeks after leaving endemic area |
| Clinical notes | Use when mefloquine/atovaquone-proguanil contraindicated or unavailable; not for treatment of acute malaria as monotherapy |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7 days |
| Clinical notes | Always combine with IV artesunate or quinine; never use as monotherapy; per NVBDCP guidelines |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg once daily OR 50 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 50–100 mg once daily |
| Maximum dose | 100 mg/day |
| Duration | 6–12 weeks (reassess; avoid prolonged use >3–4 months) |
| Clinical notes | Second-line after topical therapy fails; combine with topical retinoid and benzoyl peroxide; taper to sub-antimicrobial dose or stop once controlled |
| Parameter | Recommendation |
|---|---|
| Starting dose | 40 mg once daily (modified-release) OR 50 mg once daily (immediate-release) |
| Titration | Not applicable |
| Usual maintenance dose | 40–50 mg once daily |
| Maximum dose | 100 mg/day (if 40 mg insufficient) |
| Duration | 8–16 weeks |
| Clinical notes | Sub-antimicrobial dosing preferred to minimise resistance; combine with topical metronidazole or azelaic acid |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 7–14 days |
| Clinical notes | Covers Mycoplasma, Chlamydophila, Legionella; use as monotherapy only for mild atypical pneumonia; combine with beta-lactam for moderate–severe CAP |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | Acute: 14 days; Chronic (endocarditis): 18–24 months with hydroxychloroquine |
| Clinical notes | Chronic Q fever requires specialist management; add hydroxychloroquine to enhance intracellular killing |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily OR 200 mg once daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 10–14 days |
| Clinical notes | Alternative to streptomycin/gentamicin; per NCDC outbreak protocols; strict infection control required |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | PEP: 60 days; Cutaneous: 7–10 days |
| Clinical notes | Ciprofloxacin is alternative first-line; for inhalational/systemic anthrax, use IV doxycycline in multidrug regimen |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | 21 days |
| Clinical notes | Per NACO guidelines; azithromycin is alternative; aspirate fluctuant buboes (do not incise) |
| Parameter | Recommendation |
|---|---|
| Starting dose | 100 mg twice daily |
| Titration | Not applicable |
| Usual maintenance dose | 100 mg twice daily |
| Maximum dose | 200 mg/day |
| Duration | Minimum 3 weeks; continue until complete epithelialisation |
| Clinical notes | Endemic in parts of India; azithromycin is alternative; prolonged treatment often required |
| Parameter | Recommendation |
|---|---|
| Starting dose | 20 mg twice daily (sub-antimicrobial dose) |
| Titration | Not applicable |
| Usual maintenance dose | 20 mg twice daily |
| Maximum dose | 40 mg/day |
| Duration | Up to 9 months |
| Clinical notes | Adjunct to scaling/root planing; anti-collagenase effect at sub-antimicrobial dose; does not promote resistance |
| MRSA skin/soft tissue infection | 100 mg twice daily | 5–10 days | RCT data; Indian dermatology practice | OFF-LABEL; alternative when TMP-SMX unavailable |
|---|---|---|---|---|
|
Small intestinal bacterial overgrowth (SIBO)
|
100 mg twice daily | 7–10 days | Limited RCT data | OFF-LABEL; Specialist only; when rifaximin unavailable |
|
Early Lyme disease (if documented travel history)
|
100 mg twice daily | 14–21 days | International guidelines; rare in India | OFF-LABEL; very rare in India; confirm exposure history |
|
Ehrlichiosis / Anaplasmosis
|
100 mg twice daily | 7–14 days | Case reports; travel-related | OFF-LABEL; empiric for tick-borne illness with travel history |
|
Pleural effusion sclerotherapy
|
500 mg in 30–50 mL NS intrapleurally | Single instillation | RCTs; Indian pulmonology practice | OFF-LABEL; Specialist only; for recurrent malignant effusions |
|
Bullous pemphigoid (steroid-sparing)
|
100–200 mg/day | Months | RCT evidence (BLISTER trial) | OFF-LABEL; Specialist only; with topical steroids |
|
Chronic prostatitis (Category II/III)
|
100 mg twice daily | 4–6 weeks | Urology practice | OFF-LABEL; when atypical organisms suspected |
| Weight Category | Loading Dose (Day 1) | Maintenance Dose | Maximum Daily Dose |
|---|---|---|---|
| <45 kg | 4 mg/kg (divided q12h) | 2–4 mg/kg/day (single or divided) | 200 mg/day |
| ≥45 kg | Adult dosing applies | 100 mg once or twice daily | 200 mg/day |
| Parameter | Children ≥8 years | Children <8 years (life-threatening only) |
|---|---|---|
| Dose | 2.2 mg/kg twice daily (max 100 mg/dose) | 2.2 mg/kg twice daily (max 100 mg/dose) |
| Duration | 7 days or until afebrile 48–72 hours | 5–7 days (shortest effective course) |
| Notes | First-line per IAP/ICMR | Specialist only; benefits outweigh dental risk in severe disease |
| Parameter | Recommendation |
|---|---|
| Minimum age | ≥8 years |
| Dose | 2 mg/kg once daily (max 100 mg) |
| Duration | 1–2 days before travel through 4 weeks after |
| Notes | Alternative when atovaquone-proguanil unavailable |
| Parameter | Recommendation |
|---|---|
| Age | ≥8 years (or <8 years if benefits outweigh risks) |
| Dose | 2.2 mg/kg twice daily (max 100 mg/dose) |
| Duration | 7 days |
| Notes | Always combine with IV artesunate; never monotherapy |
| Parameter | Recommendation |
|---|---|
| Age | ≥8 years |
| Dose | 2–4 mg/kg/day in single or divided doses |
| Duration | Single dose or 3 days |
| Notes | Adjunct to ORS; reduces disease duration |
| Parameter | Recommendation |
|---|---|
| Age | Any age (including <8 years due to severity) |
| Dose | 2.2 mg/kg twice daily (max 100 mg/dose) |
| Duration | 60 days |
| Notes | Life-saving indication overrides dental concerns |
| Indication | Age | Dose | Duration | Notes |
|---|---|---|---|---|
|
Mycoplasma pneumoniae pneumonia
|
≥8 years | 2 mg/kg twice daily (max 100 mg/dose) | 7–10 days | OFF-LABEL; when macrolide-resistant suspected |
|
Acne vulgaris (moderate–severe)
|
≥12 years | 50–100 mg once daily | 6–12 weeks | OFF-LABEL; with topical therapy |
| Renal Function | Recommendation |
|---|---|
| eGFR >30 mL/min | No adjustment needed |
| eGFR 10–30 mL/min | Standard dose acceptable for short courses; avoid prolonged therapy |
| eGFR <10 mL/min | Use with caution; standard dose acceptable but monitor for accumulation |
| Haemodialysis | Not significantly removed; no supplemental dose required |
| Peritoneal dialysis | Not significantly removed; standard dosing |
| CRRT | Standard dosing; monitor clinically |
Cautions
Pregnancy
| Parameter | Details |
|---|---|
| Risk Category |
Contraindicated in 2nd and 3rd trimesters
|
| Risk Summary | Crosses placenta; causes permanent teeth discoloration (yellow-brown), enamel hypoplasia, and inhibition of bone growth in fetus |
| First Trimester | Limited data; may be used if benefits clearly outweigh risks and no alternative exists |
| Preferred Alternatives | Azithromycin (for chlamydia, atypicals), Amoxicillin (for respiratory infections), Penicillin (for syphilis), Ceftriaxone (for gonorrhoea) |
| When May Be Used | Life-threatening maternal infection with no suitable alternative (e.g., rickettsial disease) — specialist decision |
| Monitoring | If inadvertent exposure, counsel regarding risks; no specific fetal monitoring indicated |
| Parameter | Details |
|---|---|
| Compatibility |
Generally compatible for short courses
|
| Milk Levels | Low; minimal excretion into breast milk |
| Infant Absorption | Poorly absorbed by infant due to chelation with milk calcium |
| Preferred Alternatives | Azithromycin (if appropriate for indication) |
| Infant Monitoring | Observe for oral candidiasis, loose stools; theoretical dental staining risk with prolonged maternal use is very low |
| Recommendation | Short courses (≤3 weeks) acceptable during breastfeeding; avoid prolonged therapy if possible |
| Parameter | Recommendation |
|---|---|
| Starting Dose | Standard adult dosing (100 mg once or twice daily) |
| Titration | Not applicable |
| Special Considerations | Higher risk of oesophageal ulceration — ensure adequate hydration and upright posture; monitor for pill oesophagitis symptoms (dysphagia, odynophagia, retrosternal pain) |
| Renal Function | No dose adjustment typically needed |
| Drug Interactions | Review concurrent medications (antacids, iron, calcium supplements, anticoagulants) |
| Adverse Effects | Monitor for Clostridioides difficile infection; may be more susceptible |
| Interacting Drug | Effect | Mechanism | Recommendation |
|---|---|---|---|
|
Isotretinoin / Acitretin
|
Risk of benign intracranial hypertension (pseudotumour cerebri) | Additive effect on intracranial pressure |
AVOID combination
|
|
Methotrexate
|
Increased methotrexate toxicity | Decreased renal clearance; displaced protein binding |
Avoid or use with extreme caution; monitor closely
|
|
Warfarin / Acenocoumarol
|
Enhanced anticoagulant effect; increased bleeding risk | Altered gut flora reducing vitamin K synthesis; possible CYP inhibition |
Monitor INR closely; may need warfarin dose reduction
|
|
Ciclosporin
|
Increased ciclosporin levels | Unknown mechanism |
Monitor ciclosporin levels
|
|
Antacids (Al/Mg/Ca-containing)
|
Markedly reduced doxycycline absorption | Chelation in GI tract |
Separate by at least 2–3 hours
|
|
Oral iron preparations
|
Reduced absorption of both drugs | Mutual chelation |
Separate by at least 2–3 hours
|
|
Calcium supplements / Dairy
|
Reduced doxycycline absorption | Chelation |
Separate by 2 hours; or take doxycycline with low-calcium meal
|
|
Sucralfate
|
Reduced doxycycline absorption | Physical binding |
Separate by at least 2 hours
|
|
Quinapril
|
Reduced quinapril absorption | Contains magnesium carbonate excipient |
Separate administration
|
| Interacting Drug | Effect | Recommendation |
|---|---|---|
|
Rifampicin
|
Reduced doxycycline levels (half-life reduced by ~50%) | May need doxycycline 100 mg twice daily instead of once daily; monitor clinical response |
|
Phenytoin / Carbamazepine / Phenobarbital
|
Reduced doxycycline efficacy | Enzyme induction; consider higher doxycycline dose or twice daily dosing |
|
Oral contraceptives
|
Theoretical reduced efficacy (controversial) | Limited evidence; advise additional contraception during antibiotic course and 7 days after (as per standard practice) |
|
Theophylline
|
Possible increased GI adverse effects | Monitor for nausea, vomiting |
|
Digoxin
|
Possible increased digoxin levels (in ~10% patients) | Monitor digoxin levels if signs of toxicity |
|
Penicillins
|
Possible antagonism (bacteriostatic vs bactericidal) | Clinical significance uncertain; avoid in severe infections like endocarditis/meningitis if possible |
|
Lithium
|
Possible increased lithium levels | Monitor lithium levels |
|
Kaolin-pectin antidiarrhoeals
|
Reduced doxycycline absorption | Separate by 2 hours |
Serious Adverse effects
| Adverse Effect | Clinical Notes |
|---|---|
|
Benign intracranial hypertension (pseudotumour cerebri)
|
Headache, visual disturbances, papilloedema; discontinue immediately
|
|
Stevens-Johnson syndrome / Toxic epidermal necrolysis
|
Rare; discontinue immediately; hospitalisation required
|
|
Drug-induced hepatotoxicity
|
Monitor LFTs; discontinue if significant elevation |
|
Clostridioides difficile colitis
|
May occur during or weeks after therapy; discontinue and treat appropriately |
|
Severe photosensitivity / phototoxic bullous eruption
|
Discontinue; supportive care |
|
Oesophageal ulceration / stricture
|
Odynophagia, retrosternal pain; prevention is key |
|
Exacerbation of myasthenia gravis
|
Worsening weakness; avoid in known MG |
|
Hypersensitivity reactions / Anaphylaxis
|
Rare; standard management |
|
Permanent teeth discoloration
|
In children <8 years; enamel hypoplasia |
| Timing | Parameters |
|---|---|
|
Baseline
|
LFTs if prolonged course planned (>2–3 weeks); renal function (for drug interaction assessment, not dose adjustment) |
|
During Therapy
|
Clinical response; signs of oesophageal irritation; skin for photosensitivity; signs of superinfection |
|
Long-term Use (>3 months)
|
LFTs every 2–3 months; monitor for C. difficile symptoms; periodic dental check in younger patients |
|
If on Anticoagulants
|
INR within 3–5 days of starting and after stopping |
|
Symptoms of Intracranial Hypertension
|
Immediate ophthalmological evaluation if headache, visual changes, papilloedema |
| Doxt | Dr. Reddy's | Capsules 100 mg |
|---|---|---|
| Doxycee | Cipla | Capsules 100 mg |
| Doxy-1 | Micro Labs | Capsules/Tablets 100 mg |
| Microdox | Micro Labs | Capsules 100 mg |
| Doxrid | Ridley Life Sciences | Capsules 100 mg |
| Biodoxi | Biochem | Capsules 100 mg |
| Tetradox | Alkem | Capsules 100 mg |
| Doxybond | Mankind | Capsules 100 mg |
| Doxiford | Intas | Capsules 100 mg |
| Brand Name | Combination | Use |
|---|---|---|
| Doxt-SL | Doxycycline + Lactobacillus | GI protection |
| Formulation | Approximate Price | Notes |
|---|---|---|
| Capsules 100 mg (strip of 10) | ₹50–120 | Wide brand variation |
| Tablets 100 mg (strip of 10) | ₹40–100 | |
| Injection 100 mg vial | ₹80–200 | Limited use |
Clinical pearls
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