Rifampin: Difference between revisions
(Restore original dosing content alongside dynamic SMW tables) |
(Remove disease-specific dosing covered by dynamic SMW tables) |
||
| Line 17: | Line 17: | ||
===Inactive [[TB]], HIV+=== | ===Inactive [[TB]], HIV+=== | ||
*600mg PO daily for 4 months | *600mg PO daily for 4 months | ||
===[[Neisseria meningitidis|Meningococcal Prophylaxis]]=== | ===[[Neisseria meningitidis|Meningococcal Prophylaxis]]=== | ||
*600 mg PO BID for two days | *600 mg PO BID for two days | ||
| Line 27: | Line 25: | ||
*15-20mg/kg/day PO/IV in 1 or 2 divided doses for at least 6 weeks in combination with a [[tetracycline]] | *15-20mg/kg/day PO/IV in 1 or 2 divided doses for at least 6 weeks in combination with a [[tetracycline]] | ||
**MAX 600 to 900mg/day | **MAX 600 to 900mg/day | ||
===Hansen Disease=== | ===Hansen Disease=== | ||
*Paucibacillary, single lesion | *Paucibacillary, single lesion | ||
Revision as of 02:58, 20 March 2026
General
- Type: bactericidal antibiotic
- Dosage Forms: 150, 300; PO, IV
- Common Trade Names: Rifadin
Pharmacology
- Half-life: 1.5-5hours (increased if there is hepatic dysfunction)
- Rifampin autoinduces its own metabolism so half-life is decreased with subsequent dosing.
- Metabolism: Hepatic
- Excretion: Bile; Urine <30%
- Mechanism of Action: inhibits bacterial RNA synthesis
Adult Dosing
Active TB
- 10mg/kg/day (in combination with isoniazid and pyrazinamide) PO or IV for 2 months
- Then 10mg/kg/day (in combination with isoniazid) for 4 months or longer as needed
- MAX, 600mg/day
Inactive TB, HIV+
- 600mg PO daily for 4 months
Meningococcal Prophylaxis
- 600 mg PO BID for two days
Bartonellosis
- 300mg PO or IV q12h plus doxycycline
Brucellosis
- 15-20mg/kg/day PO/IV in 1 or 2 divided doses for at least 6 weeks in combination with a tetracycline
- MAX 600 to 900mg/day
Hansen Disease
- Paucibacillary, single lesion
- 600 mg PO x1 with ofloxacin and minocycline
- Paucibacillary
- 600 mg PO qmo x 6mo with dapsone
- Multibacillary
- 600 mg PO qmo x 12mo with dapsone and clofazimine
Anthrax, systemic
- 600 mg IV q12h for at least 2 wk as part of a multi-drug regimen
- Switch to PO abx x60 days total if inhalational exposure
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| Anthrax | 600 mg IV q12h for at least 2 wk as part of a multi-drug regimen; Switch to PO abx x60 days total if inhalational exposure | Anthrax, systemic |
| Brucella | 15-20mg/kg/day PO/IV in 1 or 2 divided doses for at least 6 weeks in combination with a tetracycline; MAX 600 to 900mg/day | Brucellosis |
| Cat-scratch disease | 300mg PO or IV q12h plus doxycycline | Bartonellosis |
| Ehrlichiosis | 300mg PO q12hrs | Pregnant |
| Endocarditis | 1200 mg/day PO in 2 doses | Prosthetic Valve Endocarditis (Early) |
| Infectious tenosynovitis | 600 mg PO once daily | Mycobacteria |
| Leprosy | Paucibacillary, single lesion; 600 mg PO x1 with ofloxacin and minocycline; Paucibacillary; 600 mg PO qmo x 6mo with dapsone; Multibacillary; 600 mg PO qmo x 12mo with dapsone and clofazimine | Hansen Disease |
| Neisseria meningitidis | 600 mg PO BID for two days | Neisseria meningitidis |
| Tuberculosis | 10mg/kg/day (in combination with isoniazid and pyrazinamide) PO or IV for 2 months; Then 10mg/kg/day (in combination with isoniazid) for 4 months or longer as needed; MAX, 600mg/day | Active TB |
| Tuberculosis | 600mg PO daily for 4 months | Inactive TB, HIV+ |
Pediatric Dosing
Active TB
- <15 yo
- 10-20 mg/kg PO/IV qd for at least 6mo
- Max: 600 mg/day
- 10-20 mg/kg PO/IV qd for at least 6mo
- 15+ yo
- 10 mg/kg PO/IV qd for at least 6mo
- Max: 600 mg/day
- 10 mg/kg PO/IV qd for at least 6mo
Latent TB
- <15 yo
- 10-20 mg/kg PO/IV qd x4mo
- Max: 600 mg/day
- 10-20 mg/kg PO/IV qd x4mo
- 15+ yo
- 10 mg/kg PO/IV qd x4mo
- Max: 600 mg/day
- 10 mg/kg PO/IV qd x4mo
H. influenza prophylaxis
- <1 mo
- 10mg/kg PO/IV q24h x4 days
- Max: 600 mg/day
- 10mg/kg PO/IV q24h x4 days
- 1+ mo
- 20 mg/kg PO/IV q24h x4 days
- Max: 600 mg/day
Meningcococcal prophylaxis
- <1 mo
- 5mg/kg PO/IV q24h x4 days
- Max: 600 mg/day
- 5mg/kg PO/IV q24h x4 days
- 1+ mo
- 10 mg/kg PO/IV q24h x4 days
- Max: 600 mg/day
Endocarditis, Staphylococcal prosthetic valve
- 20 mg/kg/day PO/IV divided q8h for at least 6wk with gentamicin and nafcillin
- Max 900 mg/day
Hansen Disease
- Paucibacillary, 10-14 yo
- 450mg PO qmo x6mo with dapsone
- Paucibacillary, 15+ yo
- 600 mg PO qmo x 6mo with dapsone
- Multibacillary, 10-14 yo
- 450mg PO qmo x 12mo with dapsone and clofazimine
- Multibacillary, 15+ yo
- 600 mg PO qmo x 12mo with dapsone and clofazimine
Anthrax, systemic
- Neonates >32 wk gestation
- 10-20 mg/kg/day IV divided q12-24h for at least 2 wk as part of multi-drug regimen
- 1+ mo
- 20 mg/kg/day IV divided q12h for at least 2 wk as part of multi-drug regimen
- Max: 300 mg/dose
- 20 mg/kg/day IV divided q12h for at least 2 wk as part of multi-drug regimen
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| Anthrax | Neonates >32 wk gestation; 10-20 mg/kg/day IV divided q12-24h for at least 2 wk as part of multi-drug regimen; 1+ mo; 20 mg/kg/day IV divided q12h for at least 2 wk as part of multi-drug regimen; Max: 300 mg/dose | Anthrax, systemic |
| Haemophilus influenzae | <1 mo; 10mg/kg PO/IV q24h x4 days; Max: 600 mg/day; 1+ mo; 20 mg/kg PO/IV q24h x4 days; Max: 600 mg/day | H. influenza prophylaxis |
| Leprosy | Paucibacillary, 10-14 yo; 450mg PO qmo x6mo with dapsone; Paucibacillary, 15+ yo; 600 mg PO qmo x 6mo with dapsone; Multibacillary, 10-14 yo; 450mg PO qmo x 12mo with dapsone and clofazimine; Multibacillary, 15+ yo; 600 mg PO qmo x 12mo with dapsone and clofazimine | Hansen Disease |
| Neisseria meningitidis | <1 mo; 5mg/kg PO/IV q24h x4 days; Max: 600 mg/day; 1+ mo; 10 mg/kg PO/IV q24h x4 days; Max: 600 mg/day | Meningococcal prophylaxis |
| Tuberculosis | <15 yo; 10-20 mg/kg PO/IV qd for at least 6mo; Max: 600 mg/day; 15+ yo; 10 mg/kg PO/IV qd for at least 6mo; Max: 600 mg/day | Active TB |
| Tuberculosis | <15 yo; 10-20 mg/kg PO/IV qd x4mo; Max: 600 mg/day; 15+ yo; 10 mg/kg PO/IV qd x4mo; Max: 600 mg/day | Latent TB |
Special Populations
- Pregnancy Rating: C
- Lactation: Infant risk minimal
- Renal Dosing:
- Adult
- CrCl <50: Consider decreasing dose 0-50%
- HD/PD: No supplment
- Pediatric
- CrCl <50: Consider decreasing dose 0-50%
- HD/PD: No supplment
- Adult
- Hepatic Dosing
- Adult
- Avoid Use
- Pediatric
- Avoid Use
- Adult
Contraindications
- Allergy to class/drug
- IM or SC administration
- Concomitant use with atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, rilpivirine or elvitegravir/cobicistat
Adverse Reactions
Serious
- Agranulocytosis
- DIC
- Hepatotoxicity
- Nephrotoxicity
- Thrombocytopenia
- Leukopenia
- Anemia
- Porphyria exacerbation
- Erythema multiforme
- Stevens-Johnson Syndrome
- Toxic epidermal necrolysis
- C. Diff associated diarrhea
- Psychosis
- Uveitis
Common
- Reddish-Orange body fluids
- Nausea/vomiting
- Diarrhea
- Headache
- Dizziness
- Fatigue
- Disequilibrium
- Weakness
- Pruritus
- Flushing
- Anorexia
- Abdominal pain
- Dyspnea
- Contact lens staining
Acute Overdose
- Diarrhea is unique to rifampin toxicity in comparison to other antituberculous medications[1]
Antibiotic Sensitivities[2]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
