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R-Cin

✅ Treats tuberculosis
✅ Prevents bacterial growth
✅ Shortens treatment duration
✅ Lowers risk of transmission
✅ Reduces drug resistance

R-Cin contains Rifampicin.

Medisch beoordeeld door Morgan Ellis — Apotheekonderzoeker · 8 jaar ervaring  · Laatst beoordeeld: mei 2026

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⚡ Quick Answer — What is R-Cin?

R-Cin bevat rifampicin (300 mg / 450 mg / 600 mg capsules) from a WHO-GMP certified manufacturer (made by Cipla) — a bactericidal anti-tuberculous antibiotic that inhibits bacterial DNA-dependent RNA polymerase. Standard adult dose for active TB: 10 mg/kg once daily (typically 450 mg for 38–55 kg, 600 mg for > 55 kg) op een lege maag — one hour before food or two hours after. Rifampicin is never used alone for active TB; it is always combined with isoniazid, pyrazinamide, and ethambutol (the 4-drug RIPE regimen) for the first two months, then continued with isoniazid for four more months. Single-agent rifampicin has defined uses in latent TB infection (4-month monotherapy), leprosy, meningococcal contact prophylaxis, MRSA bone/joint infections, and brucellosis. Expect orange-red discolouration of urine, sweat, tears and saliva (harmless but permanently stains soft contact lenses). Rifampicin is a very potent CYP3A4/2C9/2C19 inducer and reduces the effectiveness of dozens of medications including oral contraceptives, warfarin, DOACs, statins, methadone, immunosuppressants, antiretrovirals, and many others.

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Critical safety notice — rifampicin alone is not a treatment for active tuberculosis. Active pulmonary or extrapulmonary TB requires combination therapy. The standard WHO-recommended regimen is 2 months of intensive-phase RIPE (rifampicin + isoniazid + pyrazinamide + ethambutol) followed by 4 months of continuation-phase RH (rifampicin + isoniazid). Using rifampicin as a single agent for active TB causes rapid emergence of rifampicin resistance, treatment failure, prolonged infectivity, and the development of multidrug-resistant TB (MDR-TB). Single-agent R-Cin is appropriate alleen when prescribed for: (a) continuation of an ongoing supervised combination regimen, (b) latent TB infection (4-month rifampicin monotherapy — the 4R regimen), (c) one of the defined non-TB indications listed below. If you have suspected or confirmed active TB, you need full combination therapy under specialist supervision — do not treat with rifampicin alone.

What R-Cin (Rifampicin) Is

R-Cin is the Cipla brand of rifampicin, a semi-synthetic rifamycin antibiotic introduced in the late 1960s and on the WHO Model List of Essential Medicines. Each opaque red-and-maroon capsule contains 300 mg, 450 mg, or 600 mg of rifampicin. Rifampicin is bactericidal against Mycobacterium tuberculosis, M. leprae, and a range of staphylococci, neisseria, and other intracellular pathogens. It is the most important sterilising drug in modern short-course TB therapy — the single agent that allowed treatment duration to drop from 18–24 months to 6 months in the 1970s.

How R-Cin Works (Mechanism)

Rifampicin binds to the β-subunit of bacterial DNA-dependent RNA polymerase, blocking the initiation of RNA transcription. Mammalian RNA polymerases are not affected because their structure differs at the rifampicin-binding pocket. The drug penetrates host cells, granulomas, abscess cavities, and cerebrospinal fluid in inflamed meninges — which is why it is so important against intracellular and partition-resistant infections. Resistance arises through point mutations in the rpoB gene encoding the polymerase β-subunit; this is why rifampicin must always be combined with at least one other active agent when treating organisms with high bacillary load (such as active TB).

Indications — What R-Cin Treats

1. Active tuberculosis (combination therapy only)

Rifampicin is the cornerstone of the WHO 6-month short-course regimen for drug-susceptible pulmonary and extrapulmonary TB:

FaseDuurDrugs
Intensive2 monthsRifampicin + Isoniazid + Pyrazinamide + Ethambutol (RIPE)
Continuation4 monthsRifampicin + Isoniazid (RH)

Total minimum duration is 6 months. Longer regimens (9–12 months) are used for TB meningitis, bone/joint TB, and disseminated disease. Treatment must be supervised — directly observed therapy (DOT) is recommended in most national programmes to ensure adherence and prevent the emergence of MDR-TB.

2. Latent tuberculosis infection (LTBI)

For patients with positive TB skin test or interferon-gamma release assay but no active disease, four months of rifampicin monotherapy at 10 mg/kg/day (the 4R regimen) is one of the WHO-preferred options. The 2017 NEJM trial by Menzies et al. showed 4R was non-inferior to 9 months of isoniazid and had significantly fewer hepatotoxicity events, lower discontinuation, and better completion rates. This is the only standard situation where rifampicin is correctly used as a single agent for tuberculous infection.

3. Leprosy (multibacillary multi-drug therapy)

The WHO multidrug therapy regimen for multibacillary leprosy is monthly rifampicin 600 mg + monthly clofazimine 300 mg + daily clofazimine 50 mg + daily dapsone 100 mg, for 12 months. Rifampicin is the most rapidly bactericidal agent against M. leprae — a single 600 mg dose kills more than 99% of viable organisms.

4. Meningococcal disease prophylaxis

Close contacts of a confirmed meningococcal disease case can take rifampicin 600 mg twice daily for 2 days (adults; weight-adjusted in children) to eradicate nasopharyngeal carriage. Ciprofloxacin 500 mg single dose or ceftriaxone 250 mg IM single dose are equally acceptable alternatives, particularly when rifampicin would interact with ongoing medication.

5. Staphylococcal bone, joint, and prosthetic-device infections

Rifampicin is added to vancomycin, daptomycin, or beta-lactams for serious staphylococcal infections involving biofilm — particularly prosthetic joint infections and infective endocarditis on prosthetic valves. Rifampicin penetrates biofilm where most antibiotics cannot. It must always be combined to prevent rapid resistance.

6. Brucellosis

Rifampicin 600–900 mg/day combined with doxycycline 100 mg twice daily for 6 weeks is one of the standard WHO regimens for non-complicated brucellosis. An aminoglycoside (streptomycin or gentamicin) is added for spondylitis or endocarditis.

Dosering

IndicatieAdult dosePaediatric dose
Active TB (in combination)10 mg/kg once daily, max 600 mg
 • 38–55 kg → 450 mg
 • > 55 kg → 600 mg
15 mg/kg once daily, max 600 mg
Latent TB (4R)10 mg/kg once daily for 4 months15 mg/kg once daily for 4 months
Leprosy (multibacillary)600 mg once monthly × 12 months10 mg/kg once monthly
Meningococcal prophylaxis600 mg twice daily for 2 days10 mg/kg twice daily × 2 days (max 600 mg/dose)
Bone/joint/prosthetic-device infection300–600 mg twice daily, in combinationSpecialist-led
Brucellosis (with doxycycline)600–900 mg once daily for 6 weeks15–20 mg/kg/day

Take on an empty stomach — one hour before food or two hours after. Food (especially fatty meals) reduces absorption by ~30%. Swallow capsules whole with water; do not break or open them.

Verplichte monitoring

Liver-function monitoring is required. Baseline ALT, AST, bilirubin and alkaline phosphatase before starting; repeat at 2 weeks, then monthly through treatment. Stop rifampicin and the companion drugs (especially isoniazid and pyrazinamide) and seek medical review if you develop: nausea or vomiting that does not settle, loss of appetite, jaundice (yellowing of skin or whites of the eyes), dark urine, pale stools, or right-upper-quadrant abdominal pain. Stop if ALT > 3× ULN with symptoms or > 5× ULN without symptoms.

Additional monitoring depending on regimen: full blood count (rifampicin can cause thrombocytopenia and rare haemolytic anaemia), urea/creatinine, sputum smear/culture (for active TB — conversion at 2 months is the main efficacy marker), HIV status (TB-HIV co-infection alters the regimen).

Bijwerkingen

Common (expected and usually harmless):

  • Orange-red discolouration of urine, sweat, tears, saliva (always — confirms absorption; permanently stains soft contact lenses)
  • Nausea, loss of appetite, abdominal discomfort — ease over the first 1–2 weeks
  • Mild rash, particularly in the first month

Zeldzaam maar belangrijk:

  • Drug-induced hepatitis (5–10% have asymptomatic transaminase rise; ~1% develop clinical hepatitis — risk higher in older patients, alcohol users, hepatitis B/C carriers, and when combined with isoniazid + pyrazinamide)
  • Flu-like syndrome — fever, chills, headache, myalgia — particularly with intermittent (twice- or thrice-weekly) dosing or after restarting
  • Thrombocytopenia, haemolytic anaemia, eosinophilia (rare; immune-mediated; stop drug)
  • Acute kidney injury (rare; usually with intermittent dosing)
  • Hypersensitivity rash, urticaria, angioedema, anaphylaxis (rare; permanent contraindication)
  • Stevens-Johnson syndrome / toxic epidermal necrolysis (very rare; permanent contraindication)

Geneesmiddelinteracties

Drug-interaction warning — rifampicin is one of the strongest CYP enzyme inducers in clinical use. It induces CYP3A4, CYP2C9, CYP2C19, CYP1A2, CYP2B6, P-glycoprotein, and many phase-II conjugation enzymes. Plasma concentrations of co-administered medicines can drop by 50–90%, with onset within 1–2 weeks and persisting 2–4 weeks after rifampicin is stopped. Tell your prescriber every medicine, supplement, and herbal preparation you take before starting rifampicin. The interactions table below covers the main classes; consult a pharmacist for any drug not listed.
Drug class / examplesInteraction with rifampicinWat te doen
Combined / progestogen-only oral contraceptives, patch, ring, implantSubstantial loss of efficacyUse barrier contraception (condoms) or copper IUD throughout and 4 weeks after
WarfarineINR drops sharply; risk of thrombosisMonitor INR weekly; expect to need a 2–3-fold dose increase; recheck weekly for 4 weeks after stopping rifampicin
DOACs (apixaban, rivaroxaban, dabigatran, edoxaban)All DOAC levels drop substantiallySwitch to warfarin (or LMWH) for the duration of rifampicin treatment
Statins (simvastatin, atorvastatin, lovastatin)Plasma levels reduced > 50%Switch to fluvastatin, rosuvastatin, or pravastatin (less affected); discuss with prescriber
HIV protease inhibitors (lopinavir, atazanavir, darunavir)PI levels collapse; ART failureSwitch rifampicin to rifabutin or change ART regimen — specialist input mandatory
HIV NNRTIs (efavirenz OK; nevirapine reduced)VariableEfavirenz-based ART is generally compatible with rifampicin
Dolutegravir, raltegravirLevels reducedDolutegravir 50 mg twice daily with rifampicin; raltegravir 800 mg twice daily
MethadoneWithdrawal within daysIncrease methadone dose 50–100% with monitoring; warn the patient before starting rifampicin
Tacrolimus, ciclosporin, sirolimus, everolimusTrough levels collapse; transplant rejection riskSpecialist transplant team input before rifampicin is started
Phenytoin, carbamazepineAnticonvulsant levels drop; seizure riskMonitor levels; dose increase often needed
Corticosteroids (prednisolone, dexamethasone)Steroid clearance roughly doublesIncrease steroid dose if treating Addison’s disease, asthma, or autoimmune flare
Itraconazole, ketoconazole, voriconazoleAntifungal levels drop dramaticallyAvoid combination — consider fluconazole (less affected) or amphotericin
Sulfonylureas (gliclazide, glimepiride, glipizide)Glycaemic control deterioratesMonitor blood glucose; dose-adjust as needed
LevothyroxineIncreased clearance; TSH risesRecheck TSH at 6 weeks; expect to increase levothyroxine dose
Theophylline, beta-blockers (metabolised), opioids (codeine, oxycodone)Reduced effectClinical monitoring; titrate to effect

This list is not exhaustive. Always have a pharmacist or physician review every concurrent medication and supplement — including over-the-counter analgesics, herbal preparations, and complementary medicines.

Contra-indicaties en voorzorgsmaatregelen

  • Known hypersensitivity to rifampicin or any rifamycin (rifabutin, rifapentine)
  • Acute liver disease, established jaundice, or chronic liver disease with significant impairment
  • Concurrent saquinavir + ritonavir (severe hepatotoxicity)
  • Porphyria (rifampicin can precipitate acute attacks)

Use with caution in: alcohol-use disorder, chronic hepatitis B or C, malnutrition (vitamin K deficiency → bleeding risk), older adults, history of drug-induced hepatitis. Diabetes management may become harder; insulin requirements often rise.

Pregnancy, Breastfeeding, and Children

Rifampicin is part of the standard WHO TB regimen used in pregnancy — the risks of untreated active TB to mother and foetus far outweigh the very small theoretical drug risk. Vitamin K 10 mg orally daily is added in the last 4 weeks of pregnancy to reduce neonatal bleeding risk. Compatible with breastfeeding (small amounts in milk; not enough to treat the baby and not enough to harm). Used in children at 15 mg/kg/day in active TB and at 10 mg/kg single-dose for meningococcal prophylaxis.

Opslag

Store at 15–30 °C in the original blister or bottle, protected from moisture and direct sunlight. Capsules are heat-sensitive — do not transfer to a pill organiser for long periods. Keep out of reach of children. Dispose of unused or expired capsules through a pharmacy take-back scheme.

Veelgestelde vragen

Can I treat active tuberculosis with R-Cin alone?

No — never. Single-agent rifampicin for active TB causes rapid resistance and treatment failure. Active TB is treated with the 4-drug RIPE regimen (rifampicin + isoniazid + pyrazinamide + ethambutol) for 2 months, then 4 months of rifampicin + isoniazid. Single-agent rifampicin is appropriate only for latent TB infection, leprosy, meningococcal prophylaxis, certain MRSA infections, and brucellosis — all under medical supervision.

Why does rifampicin turn urine, sweat and tears orange-red?

Rifampicin and its metabolites are intensely red-orange pigments excreted in all body fluids. The colour is harmless and confirms the drug is being absorbed. It can permanently stain soft contact lenses, light-coloured clothing during sweating, and bedding. Switch to glasses or daily-disposable contacts during therapy and warn your dentist (it can stain crowns and dentures temporarily).

How should R-Cin be taken — with food or empty stomach?

Take R-Cin on an lege maag: one hour before food or two hours after. Food — particularly high-fat meals — reduces rifampicin bioavailability by roughly 30%, which can drop blood levels below the therapeutic range. If empty-stomach dosing causes intolerable nausea, a small light snack (a couple of plain biscuits) is preferable to skipping or vomiting the dose. Take the full daily dose at one time, not split.

Will rifampicin make my contraceptive pill stop working?

Yes. Rifampicin reduces ethinyl-oestradiol and progestogen levels through hepatic enzyme induction; combined and progestogen-only pills, the patch, the vaginal ring, and progestogen implants are all unreliable during rifampicin therapy and for at least 4 weeks after stopping. Use barrier contraception (condoms) or a non-hormonal method (copper IUD) throughout. The depot injection (DMPA) and the levonorgestrel intrauterine system are considered unaffected.

Can I drink alcohol while on R-Cin?

Avoid alcohol or limit it strictly. Both rifampicin and the companion drug isoniazid are hepatotoxic, and alcohol substantially increases the risk of drug-induced hepatitis — one of the main reasons TB treatment has to be stopped. Daily alcohol use is a relative contraindication to standard regimens; tell your physician before starting.

What blood tests should I have during rifampicin therapy?

Baseline before starting: liver function tests (ALT, AST, bilirubin, alkaline phosphatase), full blood count, urea/creatinine. Repeat liver function at 2 weeks, then monthly throughout therapy — or sooner if you develop nausea, jaundice, dark urine, or right-upper-quadrant pain. Stop rifampicin (and isoniazid) and contact your physician if ALT exceeds three times the upper limit of normal with symptoms, or five times without symptoms.

Is R-Cin safe in pregnancy and breastfeeding?

Active TB in pregnancy is dangerous to both mother and foetus, and rifampicin is one of the agents considered safe in pregnancy — the WHO and most national TB programmes recommend it as part of the standard regimen. Vitamin K (10 mg orally daily) is added in the last 4 weeks of pregnancy to reduce neonatal haemorrhage risk. Rifampicin passes into breast milk in small amounts but is compatible with breastfeeding. All decisions should be made with an obstetrician and TB specialist.

What is the difference between rifampicin and rifaximin?

Both are members of the rifamycin class but they are clinically very different. Rifampicine is well absorbed systemically, used for tuberculosis, leprosy and serious bacterial infections, and is a major CYP enzyme inducer. Rifaximin is virtually non-absorbable, stays in the gut, and is used for traveller’s diarrhoea, hepatic encephalopathy, and IBS-D — it has minimal systemic side effects and minimal drug interactions. They are not interchangeable.

I am on antiretroviral therapy for HIV — can I still take rifampicin?

This needs specialist input. Rifampicin dramatically reduces blood levels of HIV protease inhibitors and several non-nucleoside reverse transcriptase inhibitors, risking ART failure and HIV resistance. Common workarounds: switch rifampicin to rifabutin (a less potent inducer), choose an ART regimen compatible with rifampicin (efavirenz-based regimens, or dolutegravir at twice-daily dosing), or sequence the treatments. Never start rifampicin without reviewing your ART regimen with the HIV physician.

How is R-Cin stored?

Store at 15–30 °C in the original packaging, protected from moisture, heat, and direct sunlight. Keep away from children — rifampicin overdose causes red discolouration of skin and severe hepatotoxicity. Dispose of expired or unused stock through a pharmacy take-back scheme rather than household waste.

Medical disclaimer: Information on this page is intended for adults under medical supervision. Active tuberculosis is a serious, notifiable infectious disease that requires combination antibiotic therapy, expert specialist supervision, contact tracing, and directly observed treatment in many jurisdictions. Do not self-treat active TB. Discuss any anti-tuberculous medication, dose change, or planned discontinuation with a qualified physician. If you experience jaundice, dark urine, severe abdominal pain, sudden vision change or loss of red-green colour discrimination, severe rash, or signs of severe allergic reaction, seek emergency care immediately.

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