
Tergocin200 mg/via
Incepta Pharmaceuticals Ltd.
Teicoplanin is a glycopeptide antibiotic indicated for the treatment of serious infections caused by susceptible Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and more.
Teicoplanin is a glycopeptide antibiotic indicated for the treatment of serious infections caused by susceptible Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), particularly when penicillins or cephalosporins are inappropriate, ineffective, or not tolerated.
Clostridioides difficile-associated diarrhoea/colitis (oral Teicoplanin) has been used off-label as an alternative to oral vancomycin in some settings, though this is not a primary approved indication everywhere.
Teicoplanin should only be used for infections confirmed or strongly suspected to be caused by susceptible Gram-positive organisms; it is not effective against Gram-negative bacteria.
Teicoplanin is administered by intravenous (IV) bolus injection over 3-5 minutes, IV infusion over about 30 minutes, or by intramuscular (IM) injection, according to the clinical situation. Dosing typically begins with loading doses to rapidly achieve therapeutic plasma concentrations, followed by a once-daily maintenance dose.
| Indication | Loading dose | Maintenance dose |
|---|---|---|
| Moderate infections (e.g., skin/soft tissue, uncomplicated UTI) | 400 mg IV on day 1 | 200 mg once daily IV/IM |
| Severe infections (bone/joint, pneumonia, endocarditis, bacteraemia) | 400 mg IV every 12 hours for 3-5 doses | 400 mg once daily IV/IM (up to higher doses in some severe/endocarditis cases per specialist guidance) |
| CAPD-associated peritonitis | As directed by treating physician (systemic and/or intraperitoneal use) | Individualised |
| Surgical prophylaxis | 400 mg IV as a single dose at induction of anaesthesia | Not applicable |
No dose adjustment is usually needed for the first 3-4 days of therapy. From day 4 onward, maintenance dose adjustment based on creatinine clearance (CrCl) is required: approximately half the normal maintenance dose for moderate renal impairment (CrCl about 40-60 mL/min) and about one-third of the normal maintenance dose (or dosing every 2-3 days) for severe renal impairment (CrCl below 40 mL/min) or patients on haemodialysis. Therapeutic drug monitoring is recommended where available, especially in renal impairment and prolonged therapy.
Important: Take Teicoplanin exactly as prescribed by your physician; do not stop, extend, skip doses, or share this medicine with others without medical advice, as inappropriate use can lead to treatment failure and antibiotic resistance.
Most patients tolerate Teicoplanin well, but as with any antibiotic, side effects can occur.
Seek prompt medical attention for signs of a serious allergic reaction (swelling of the face/throat, difficulty breathing, severe rash), unusual bleeding or bruising, significant reduction in urine output, or new hearing/balance problems while receiving Teicoplanin.
Teicoplanin is contraindicated in patients with a known history of hypersensitivity (allergic reaction) to Teicoplanin itself.
Cross-sensitivity with vancomycin (another glycopeptide) can occur, but is not universal; therefore, patients with a known vancomycin allergy are not automatically excluded from receiving Teicoplanin, but it should be used with heightened caution and close monitoring in this population rather than being treated as an absolute contraindication.
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.