Compatibility «Clarithromycin» and «Liprimar»
Between «Clarithromycin» and «Liprimar» found 3 dangerous and 19 negative interactions, joint admission is not recommended without consulting a doctor.
Interaction tableCompare |
Liprimar |
| ✘Clarithromycin Analogs | |
| ✘Liprimar [Atorvastatin and more 1Atorvastatin calcium] Analogs |
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Interactions Clarithromycin with Liprimar
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Dangerous interactions
- During treatment with HMG-CoA reductase inhibitors with simultaneous use of cyclosporine, fibrates, nicotinic acid in lipid-lowering doses (more than 1 g/ day) or inhibitors of the CYP3A4 isoenzyme (e.g. erythromycin, clarithromycin, antifungal agents - azole derivatives) increase the risk of myopathy (see 'Special instructions').
- With simultaneous administration of HMG-CoA reductase inhibitors (lovastatin, simvastatin), acute skeletal muscle necrosis is possible.
- Concomitant administration of clarithromycin with lovastatin and simvastatin is contraindicated (see section 'Contraindications') due to the fact that these statins are largely metabolized by the CYP3A4 isoenzyme, and co-administration with clarithromycin increases their serum concentrations, which leads to an increased risk of myopathy, including rhabdomyolysis.
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Negative interactions
- Inhibitors of the CYP3A4 isoenzyme.
- Since atorvastatin is metabolized by the CYP3A4 isoenzyme, the combined use of atorvastatin with inhibitors of the CYP3A4 isoenzyme may lead to an increase in the concentration of atorvastatin in blood plasma.
- It has been found that powerful inhibitors of the CYP3A4 isoenzyme lead to a significant increase in the concentration of atorvastatin in blood plasma.
- If possible, the simultaneous use of potent inhibitors of the CYP3A4 isoenzyme (for example, cyclosporine, telithromycin, clarithromycin, delavirdine, stiripentol, ketoconazole, voriconazole, itraconazole, posaconazole and HIV protease inhibitors, including ritonavir, lopinavir, atazanavir, indinavir, darunavir) should be avoided.
- Moderate inhibitors of the CYP3A4 isoenzyme (e.g. erythromycin, diltiazem, verapamil and fluconazole) may lead to an increase in the concentration of atorvastatin in blood plasma.
- It is known that both amiodarone and verapamil inhibit the activity of the CYP3A4 isoenzyme and the simultaneous use of these drugs with atorvastatin may lead to increased exposure to atorvastatin.
- In this regard, it is recommended to reduce the maximum dose of atorvastatin and conduct appropriate monitoring of the patient's condition while using moderate inhibitors of the CYP3A4 isoenzyme.
- With the simultaneous use of atorvastatin and erythromycin (500 mg 4 times a day) or clarithromycin (500 mg 2 times a day), inhibitors of the CYP3A4 isoenzyme, an increase in the concentration of atorvastatin in blood plasma was observed (see 'Special instructions').
- Simultaneous use of atorvastatin with protease inhibitors, known as CYP3A4 isoenzyme inhibitors, is accompanied by an increase in the concentration of atorvastatin in blood plasma.
- Since grapefruit juice contains one or more components that inhibit the CYP3A4 isoenzyme, excessive consumption (more than 1.2 liters per day) can cause an increase in the concentration of atorvastatin in blood plasma.
- The combined use of atorvastatin with inducers of the CYP3A4 isoenzyme (for example, efavirenz, rifampicin or St. John's wort preparations) may lead to a decrease in the concentration of atorvastatin in blood plasma.
- Due to the dual mechanism of interaction with rifampicin (an inducer of the CYP3A4 isoenzyme and an inhibitor of the hepatocyte transport protein OATP1B1), simultaneous use of atorvastatin and rifampicin is recommended, since delayed administration of atorvastatin after taking rifampicin leads to a significant decrease in the concentration of atorvastatin in blood plasma.
- Clarithromycin should be used with caution in combination therapy with other statins.
- If necessary, it is recommended to take the lowest dose of statin together.
- It is recommended to use statins that do not depend on the metabolism of the CYP3A isoenzyme (for example, fluvastatin).
- It is possible to interact with simultaneous use of atorvastatin with CYP3A4 inhibitors such as grapefruit juice, some macrolide antibiotics (e.g. erythromycin, clarithromycin), immunosuppressants (cyclosporine), azole antifungal drugs (e.g. itraconazole, ketoconazole), vector inhibitors, HIV and hepatitis C protease inhibitors, letermovir or the antidepressant nefazodone.
- Cyclosporine is an inhibitor of OATP1B1, OATP1B3, multidrug resistance protein (MDR1) and BCRP, as well as CYP3A4, therefore it increases the exposure of atorvastatin.
- Simultaneous use of atorvastatin and CYP3A4 inducers (e.g. efavirenz, rifampicin) may lead to a variable decrease in the concentration of atorvastatin in blood plasma.
- As a result of the dual mechanism of action of rifampicin (induction of CYP3A4 and inhibition of the OATP1B1 transporter), simultaneous co-administration of atorvastatin and rifampicin, etc. is recommended; delayed intake of atorvastatin after administration of rifampicin was associated with a significant decrease in the concentration of atorvastatin in blood plasma.
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Positive interactions
- The degree of interaction and the potentiation effect are determined by the variability of the effect on the CYP3A4 isoenzyme.
- In addition, there was an increase in the concentration of atorvastatin when used concomitantly with HIV protease inhibitors (combinations of lopinavir and ritonavir, saquinavir and ritonavir, darunavir and ritonavir, fosamprenavir, fosamprenavir with ritonavir and nelfinavir), hepatitis C protease inhibitors (boceprevir), clarithromycin and itraconazole.
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Unclear interactions
- Erythromycin/clarithromycin.
- Inducers of the CYP3A4 isoenzyme.
- HMG-CoA reductase inhibitors (statins).
- Atorvastatin is metabolized with the participation of the CYP3A4 isoenzyme.
- Macrolide antibiotics (azithromycin, clarithromycin, erythromycin).
- Clarithromycin and erythromycin are inhibitors of CYP3A4.
- With simultaneous use of atorvastatin (10 mg 1 time per day) and clarithromycin (500 mg 2 times per day) and atorvastatin monotherapy, the ratio of AUC and max'>Cmax atorvastatin was 1.82 and 1.56, respectively.
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Dangerous interactions
Decoding the colors of interactions and contraindications
| Dangerous | — | a pronounced negative interaction or contraindication. |
| Negative | — | negative interaction or side effect that may reduce effectiveness. |
| Positive | — | the interaction can SOMETIMES be used as a positive (often a dose adjustment is needed), or it is an indication. |
| No | — | the drugs do NOT interact, which is separately indicated in the instructions. |
| Unclear | — | the system failed to pre-assess the danger. |
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Additional information
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- The use of information about interactions is only possible as an introduction. This information should not be used to adjust therapy without consulting a specialist.
- The article is written: artificial intelligence Kiberis
- Sources: official instructions for medicines and their active substances, as well as inter-group interactions described in medical studies and textbooks.
- Total analyzed: 170,041,552 possible combinations of drugs and their components were found 412,577 interacting combinations.
- Medicine section: Standard evidence-based medicine
- The date of the last update of the interaction database: 2026-06-18
Category - medicine