Compatibility «Metamizole sodium+Pitofenone+Fenpiverinium bromide» and «Ciclosporin»
Between «Metamizole sodium+Pitofenone+Fenpiverinium bromide» and «Ciclosporin» found 2 dangerous and 8 negative interactions, joint admission is not recommended without consulting a doctor.
Interaction tableCompare |
Ciclosporin |
| ✘Metamizole sodium+Pitofenone+Fenpiverinium bromide [Metamizole sodium and more 2Pitofenone, Fenpiverinium bromide] Analogs | |
| ✘Ciclosporin Analogs |
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Interactions Metamizole sodium+Pitofenone+Fenpiverinium bromide with Ciclosporin
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Dangerous interactions
- Increases the risk of myopathy and rhabdomyolysis when prescribing lipid-lowering drugs (HMG-CoA reductase inhibitors), impaired renal function - against the background of aminoglycosides, amphotericin B, trimethoprim, co-trimoxazole, ciprofloxacin, some cephalosporins, NSAIDs, propafenone.
- Cyclosporine (L04AD01) + NSAIDs — Coxibs. NSAIDs are Oxycams. NSAIDs are Phenamates. NSAIDs are Pyrazolones. NSAIDs — Butylpyrazolidines(S01BC,M01A, M01B) => Nephrotoxicity increases. (A dangerous combination, it must be avoided).
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Negative interactions
- Metamizole sodium can reduce the concentration of cyclosporine in the blood serum, therefore, when using a combination of metamizole sodium + pitophenone + fenpiverinium bromide with cyclosporine, cyclosporine concentrations should be monitored.
- With myelotoxic drugs.
- Reduces the concentration of cyclosporine in plasma.
- The combined use of metamizole with CYP2B6 and/or CYP3A4 substrates, such as bupropion and efavirenz, methadone, cyclosporine, tacrolimus or sertraline, may lead to a decrease in the concentration of these drugs in blood plasma.
- Therefore, caution is recommended when using metamizole and CYP2B6 and/or CYP3A4 substrates simultaneously; assessment of the clinical response and / or concentration of the drug in blood plasma should be accompanied by therapeutic drug monitoring.
- Phenytoin, carbamazepine, barbiturates, benzodiazepine derivatives, aminoglutetimide, estrogen-progestogenic drugs, progesterone, rifampicin, isoniazid, sodium metamizole weaken the effect - accelerate elimination.
- with drugs with nephrotoxic effects: aminoglycosides (including gentamicin, tobramycin), amphotericin B, ciprofloxacin, mannitol, melphalan, co-trimoxazole (trimethoprim + sulfamethoxazole), vancomycin, nonsteroidal anti‑inflammatory drugs (including diclofenac, indomethacin, naproxen, sulindac), blockers H2-histamine receptors (including cimetidine, ranitidine), methatrexate with tacrolimus, etc.
- Nonsteroidal anti-inflammatory drugs with a pronounced 'first pass' effect through the liver (for example, diclofenac) should be used in lower doses than in patients who do not receive cyclosporine.
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Unclear interactions
- With cyclosporine.
- With CYP2B6 and/or CYP3A4 substrates.
- Metamizole can induce the metabolizing enzymes CYP2B6 and CYP3A4.
- With the simultaneous use of nonsteroidal anti-inflammatory drugs with a less pronounced 'first pass' effect (for example, acetylsalicylic acid) with cyclosporine, an increase in their bioavailability is not expected.
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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. |
Video instruction
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: 170,027,037 possible combinations of drugs and their components were found 412,563 interacting combinations.
- Medicine section: Standard evidence-based medicine
- The date of the last update of the interaction database: 2026-01-01
Category - medicine