1. Azithromycin Dihydrate
2. Pharmacological Class: Azalide Macrolide Antibiotic (Bacteriostatic 50S Ribosomal Subunit Protein Synthesis Inhibitor; WHO 'Watch' Group) • 3. Therapeutic Category: Antimicrobials — Antibacterial & Antibiotic Agents (Ch 08)
4. Clinical Overview & Verified Formulation Identity
Azithromycin Dihydrate
Code: [8.3] | Stable ID: TIP-MED-000131
Azee (Cipla), Azithral (Alembic), Zithromax (Pfizer)
Oral Film-Coated Tablets: 250 mg, 500 mg; Oral Suspension: 100 mg/5 mL, 200 mg/5 mL; IV Infusion: 500 mg/vial
Route: Oral / Parenteral / Topical as specified by formulation
Schedule H Prescription Drug • NLEM 2022 Core Essential Medicine
True
5 & 6. Mechanism of Action & Pharmacodynamics
Reversibly binds to the 23S rRNA of the bacterial 50S ribosomal subunit near the peptidyltransferase centre and blocks the polypeptide exit tunnel, inhibiting aminoacyl-tRNA translocation and bacterial protein synthesis. Primarily bacteriostatic (bactericidal at high concentrations against S. pyogenes and H. influenzae) with a pronounced post-antibiotic effect.
8. Therapeutic Indications
- Community-acquired atypical pneumonia (Mycoplasma, Chlamydophila, Legionella) and acute bacterial sinusitis/otitis
- Uncomplicated enteric fever (Salmonella Typhi/Paratyphi — oral step-down or outpatient therapy in India)
- Sexually transmitted Chlamydia trachomatis urethritis/cervicitis, scrub typhus (pregnancy alternative), and trachoma
10. Dosage and Administration (Educational Reference Summary)
Administration & Timing: Oral (once daily) or IV infusion over at least 60 minutes (never give as IV bolus or IM).
11 & 13. Contraindications, Precautions and Warnings
- History of cholestatic jaundice or hepatic dysfunction with prior macrolide use
- Hypersensitivity to Azithromycin, Erythromycin, or any macrolide/ketolide
Contraindicated if previous history of Azithromycin-associated cholestatic hepatitis; use caution in severe cirrhosis.
7, 12, 14–18. Detailed Pharmacokinetics, Interactions, Special Populations & Counselling
7 & 16. Pharmacokinetics (ADME) & Renal / Hepatic Considerations
7. Pharmacokinetics (Absorption, Distribution, Metabolism, Excretion): Absorption, distribution, metabolism, and excretion follow class pharmacokinetic profile; verify patient renal/hepatic function.
16a. Renal Considerations: No dose adjustment required in mild-to-severe renal impairment (use caution if eGFR < 10 mL/min).
16b. Hepatic Considerations: Contraindicated if previous history of Azithromycin-associated cholestatic hepatitis; use caution in severe cirrhosis.
12 & 14. Adverse Effects & Drug Interactions
- Gastrointestinal cramps, nausea, diarrhoea (motilin receptor agonism — significantly milder than Erythromycin)
- QTc interval prolongation and rare polymorphic ventricular tachycardia (Torsades de Pointes)
- Rare reversible sensorineural hearing loss / tinnitus (with high-dose prolonged courses) or cholestatic hepatitis
- QT-prolonging drugs (Ondansetron, Fluoroquinolones, Amiodarone, Domperidone, Hydroxychloroquine): additive QTc prolongation and Torsades de Pointes risk
- Aluminium/Magnesium Antacids: reduce peak plasma Cmax by ~24% (separate by 2 hours)
- Digoxin: inhibits intestinal P-gp and gut flora inactivation, raising serum digoxin levels
15, 17 & 18. Special Populations, Clinical Monitoring & Patient Counselling
15. Use in Special Populations (Pregnancy, Lactation, Paediatrics, Geriatrics): Evaluate maternal-foetal benefit-risk ratio, paediatric mg/kg ceiling, and geriatric renal function prior to prescribing.
17. Clinical & Laboratory Monitoring: Monitor clinical response, baseline renal/hepatic parameters, and relevant serum biomarkers.
18. Patient Counselling & Storage:- Complete the full prescribed 3-day or 5-day course; because Azithromycin stays in tissues for 68 hours, it continues working for several days after the last tablet.
- Separate from antacids containing aluminium or magnesium by at least 2 hours.
- Do not self-medicate for viral colds or sore throats (Watch group antibiotic).
Storage & Dispensing Notes: Store below 30°C.
Visual Pharmacology Illustration (PLATE-8.9)
19. Authoritative References & Source Traceability
Primary Reference Record: Indian Pharmacopoeia (IP 2026) • NLEM 2022 (MoHFW) • CDSCO Approved Prescribing Information
Verification Portals: Indian Pharmacopoeia Commission (IPC) • CDSCO (India Jurisdiction) • NCBI Bookshelf • DailyMed (US FDA Label Reference)
Last Reviewed Date: 2026-11-08 • Related Study Guide: Antimicrobial Stewardship & PK/PD Optimization →