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MEDICINE MONOGRAPH CODE: [7.22] ID: TIP-MED-000124

Hydroxychloroquine Sulfate (HCQ)

Active Ingredient / Scientific Identity: Hydroxychloroquine Sulfate • Class: 4-Aminoquinoline Immunomodulator & Disease-Modifying Antirheumatic Drug — DMARD (Schedule H1 / H | NLEM 2022)

⚖️ Compare Profile
Generic / Entity NameHydroxychloroquine Sulfate (HCQ) ([7.22])
Verified Indian Brands / RefGeneric Compendial Entry (No Commercial Brand Claimed)
Pharmacological Class4-Aminoquinoline Immunomodulator & Disease-Modifying Antirheumatic Drug — DMARD (Schedule
Available Dosage FormsFilm-Coated Tablets: 200 mg, 300 mg, 400 mg
Regulatory ClassificationSchedule H Prescription Drug (To be sold by retail on the prescription of a Registere
Key Warning & Review DateRenal: 50% renally cleared — reduce dose in CKD Stage 3–5 (eGFR <60 mL/min is a major risk factor for retinal toxicity!). Hep
Reviewed: 2026-11-10
Safety Matrix:⚖️ Legal Status: Schedule H Prescription Drug (To be sold by retail o✔️ Standard Clinical Dispensing Precautions

1. Clinical & Scientific Overview

Hydroxychloroquine Sulfate (HCQ) (TIP-MED-000124, Reference Code [7.22]) is classified under Pain, Inflammation, Rheumatology & Gout Medicines (Ch 07) as a 4-Aminoquinoline Immunomodulator & Disease-Modifying Antirheumatic Drug — DMARD (Schedule H1 / H | NLEM 2022). Within the Indian regulatory and compendial framework, it is governed under Schedule H Prescription Drug (To be sold by retail on the prescription of a Registered Medical Practitioner only — Drugs Rules 1945).

Verified Indian Market Examples / Compendial Status:
Representative Indian Market Examples (Edition 2.7 Ch 07 [7.22], p. 89): HCQS (Ipca), Zyq (Zydus), Oxiklorin (Wallace), Plaquenil — Strengths & Dosage Forms: Film-Coated Tablets: 200 mg, 300 mg, 400 mg
Representative Indian Market Examples (Edition 2.7 Ch 07 [7.22], p. 89): HCQS (Ipca), Zyq (Zydus), Oxiklorin (Wallace), Plaquenil — Strengths & Dosage Forms: Film-Coated Tablets: 200 mg, 300 mg, 400 mg
Dosage Forms & Available Strengths:
Film-Coated Tablets: 200 mg, 300 mg, 400 mg
Routes: Oral / Parenteral / Topical as specified by formulation

3. Mechanism of Action & Pharmacodynamics

4-Aminoquinoline Immunomodulator & Disease-Modifying Antirheumatic Drug — DMARD (Schedule H1 / H | NLEM 2022) acting on target receptor/enzyme pathways in Pain, Inflammation, Rheumatology & Gout Medicines (Ch 07): clinical efficacy is mediated via 4-Aminoquinoline Immunomodulator & Disease-Modifying Antirheumatic Drug — DMARD (Schedule H1 / H | NLEM 2022) for Rheumatoid arthritis (mild-to-moderate or in triple DMARD combination with Methotrexate + Sulfasalazine), Systemic Lupus Erythematosus (SLE — reduces flares, thrombosis, and mortality; safe & continued throughout pregnancy in SLE!), Sjogren's syndrome; also approved in India as 3rd/4th-line add-on in Type 2 DM.

4. Therapeutic Indications & Evidence-Supported Uses

  • Rheumatoid arthritis (mild-to-moderate or in triple DMARD combination with Methotrexate + Sulfasalazine), Systemic Lupus Erythematosus (SLE — reduces flares, thrombosis, and mortality
  • safe & continued throughout pregnancy in SLE!), Sjogren's syndrome
  • also approved in India as 3rd/4th-line add-on in Type 2 DM

🇮🇳 Jurisdiction & Indication Note: Indications and schedules reflect Indian compendial and regulatory records (CDSCO / Indian Pharmacopoeia & NFI / NLEM 2022). Where international reference labels (US FDA DailyMed / NCBI StatPearls) are cited for pharmacokinetic or mechanistic parameters, international approvals do not automatically imply CDSCO approval in India.

5. Educational Dosage Context, Formulations & Administration

Educational Dosing & Regimen Summary: 200–400 mg PO daily (MUST NOT EXCEED 5.0 mg/kg/day of actual body weight — e.g., max 200–300 mg/day if weight is 50–60 kg — to prevent bull's-eye retinal maculopathy!)

Administration & Meal Timing: Take WITH a meal or a glass of milk to minimise nausea and epigastric discomfort | Once Daily with Dinner (or 200 mg BD with Breakfast & Dinner)

6. Pharmacokinetics, Metabolism & Renal/Hepatic Adjustment

Absorption & Disposition:
Absorption, distribution, metabolism, and excretion follow class pharmacokinetic profile; verify patient renal/hepatic function.
Metabolism & Biotransformation:
Renal: 50% renally cleared — reduce dose in CKD Stage 3–5 (eGFR <60 mL/min is a major risk factor for retinal toxicity!). Hepatic: Caution in hepatic disease
Elimination & Renal Adjustment:
Renal: 50% renally cleared — reduce dose in CKD Stage 3–5 (eGFR <60 mL/min is a major risk factor for retinal toxicity!). Hepatic: Caution in hepatic disease
Hepatic Impairment Considerations:
Renal: 50% renally cleared — reduce dose in CKD Stage 3–5 (eGFR <60 mL/min is a major risk factor for retinal toxicity!). Hepatic: Caution in hepatic disease

7. Contraindications, Precautions & High-Risk Warnings

Contraindications & Red-Flag Precautions:
  • Contraindicated in pre-existing retinal maculopathy/visual field defects, 4-aminoquinoline hypersensitivity, and children <6 years (200 mg tablet not suitable for <31 kg). Caution in G6PD deficiency, psoriasis, and QTc prolongation

Key Clinical Precautions: Renal: 50% renally cleared — reduce dose in CKD Stage 3–5 (eGFR <60 mL/min is a major risk factor for retinal toxicity!). Hepatic: Caution in hepatic disease

8. Adverse Effects Profile

Common & Mechanism-Related Adverse Effects:
  • Nausea, abdominal cramps, diarrhoea, anorexia, headache, skin hyperpigmentation, pruritus
  • Irreversible Bull's-Eye Retinal Maculopathy (risk increases after >5 years of use, dose >5 mg/kg/day, CKD, or concurrent Tamoxifen!), QTc prolongation / Torsades de Pointes, rare cardiomyopathy, hypoglycaemia (even in non-diabetics!), haemolysis in G6PD deficiency
Serious / Dose-Limiting Adverse Effects:
  • Monitor for severe hypersensitivity, organ toxicity, or dose-limiting adverse events.

9. Major Drug–Drug, Drug–Food & Drug–Herb Interactions

  • Additive QTc prolongation with Azithromycin, Clarithromycin, Fluoroquinolones, Ondansetron, Domperidone, Amiodarone, and Escitalopram; increases Digoxin levels (P-gp inhibition); potentiates Insulin/Sulfonylurea hypoglycaemia; Antacids reduce absorption (space by >=4h); Tamoxifen increases retinopathy risk 5-fold

10. Clinical Monitoring, Patient Counselling & Storage

Clinical & Laboratory Monitoring: Monitor clinical response, baseline renal/hepatic parameters, and relevant serum biomarkers.

Pharmacist Patient Counselling Points:

  • Patient Counselling Checklist: Take with food or milk; takes 2–3 months to relieve joint pain fully; calculate dose by body weight (<=5 mg/kg/d) and get an eye specialist retinal check-up; safe and essential to continue during pregnancy if you have Lupus (SLE); report any reading difficulty or central blurry vision immediately
  • Meal & Clock Timing Instruction: Take WITH a meal or a glass of milk to minimise nausea and epigastric discomfort (Once Daily with Dinner (or 200 mg BD with Breakfast & Dinner))
  • Missed Dose Protocol: Take with next meal if remembered; do not double dose
  • Geriatric Dispensing Pearl: Calculate mg/kg dose carefully in low-body-weight elderly Indian women (e.g., 45 kg -> max 200 mg/day!) and check eGFR

Storage, Stability & Dispensing Safeguards: Store below 25°C–30°C in original moisture- and light-resistant packaging out of reach of children. Available forms: Film-Coated Tablets: 200 mg, 300 mg, 400 mg

11. Visual Pharmacology & Mechanism Diagram (svg-v339-01-adme-12-step-journey)

THE 12-STEP ORAL DRUG JOURNEY THROUGH THE HUMAN BODY (LADME) Note: IV bolus enters Step 6 directly (F = 100%); Sublingual & Transdermal routes bypass Step 4–5 Portal First-Pass Metabolism 1. Oral Administration • Tablet / Capsule swallowed • Gastric emptying to duodenum pH 1.5–3.5 (Stomach) 2. Disintegration & Dissolution • Tablet breaks into granules • API dissolves in GI fluid Noyes-Whitney Dissolution Rate 3. GI Epithelial Absorption • Crosses intestinal villi • Passive / Active / P-gp efflux Small Intestine (Large Surface Area) 4. Portal Circulation • Mesenteric veins → Portal vein • Delivers blood to liver sinusoids Pre-systemic Venous Conduit 5. First-Pass Metabolism • Gut & hepatic CYP450 extraction • High: GTN, Propranolol, Morphine Determines Bioavailability (F = f_a × (1-E_H)) 6. Systemic Circulation • Hepatic vein → IVC → Heart • Unbound vs Albumin-bound drug Only FREE drug is active 7–8. Tissue Distribution (Vd) • Capillary permeation to organs • Blood-Brain & Placental barriers Vd = Dose / C_0 (L or L/kg) 9. Target Site of Action • Receptors (GPCR, Ion channel) • Enzymes & Carrier Transporters Pharmacodynamic Effect (E_max, EC50) 10. Hepatic Biotransformation • Phase I (CYP450 Oxidation/Hydrolysis) • Phase II (Glucuronidation/Sulfation) Converts lipophilic drug → hydrophilic metabolite 11. Renal & Biliary Elimination • Nephron: Filtration + Secretion − Reabsorption • Biliary excretion & Enterohepatic recycling Total Clearance CL_tot = CL_renal + CL_hepatic 12. Excretion from the Body • Urine (Primary polar metabolite route) • Bile/Faeces, Expired Air, Sweat, Milk Elimination Half-Life t1/2 = (0.693 × Vd) / CL
svg-v339-01-adme-12-step-journey — 8.1 Complete 12-Step Journey of an Orally Administered Drug (ADME): Figure 8.1: The 12-step physiological journey of a typical orally administered solid dosage form through Liberation, Absorption, Distribution, Metabolism, and Excretion (LADME). Note: Parenteral (IV), sublingual, and inhalational routes bypass gastrointestinal absorption and/or hepatic first-pass metabolism.

12. Authoritative References, Regulatory Sources & Editorial Disclaimer

Primary Compendial & Guideline Reference: Indian Pharmacist Desk Reference — Professional Edition 2.7 (2026–27) • Ch 07 [7.22] (p. 89)

Official Verification Portals: Indian Pharmacopoeia Commission (IPC) & National Formulary of India (NFI) • Central Drugs Standard Control Organization (CDSCO) • Ministry of Health & Family Welfare — NLEM 2022 • NCBI Bookshelf / StatPearls Pharmacology Reference • DailyMed (US FDA Official Prescribing Reference)

Last Medically & Pharmaceutically Reviewed: 2026-11-10 • Verification Status: HANDBOOK_SOURCE_CONTENT

Educational & Clinical Disclaimer: This reference profile is published solely for pharmacy education, academic study, and professional clinical reference. It does not substitute for patient-specific clinical judgement, qualified specialist oncology/medical supervision, or official CDSCO/IP prescribing information. Never self-medicate with prescription, Schedule H/H1/X, NDPS, or oncology medicines.