Aprepitant Sandoz, 125 mg, hard capsules + Aprepitant Sandoz, 80 mg, hard capsules
Aprepitantum
Aprepitant Sandoz contains the active substance aprepitant, a medicine from the group of so-called neurokinin 1 (NK1) receptor antagonists. In the brain, there is a specific area responsible for feeling nausea and vomiting. Aprepitant Sandoz blocks the signals to this area, reducing nausea and vomiting. The medicine is used in adults and adolescents from 12 years of age together with other medicinesto prevent nausea and vomiting caused by chemotherapy (cancer treatment) that causes severe and moderate nausea and vomiting (treatment with such medicines as cisplatin, cyclophosphamide, doxorubicin, or epirubicin).
Before taking Aprepitant Sandoz, discuss it with your doctor or pharmacist.
Aprepitant Sandoz 80 mg and 125 mg should not be used in children under 12 years of age, as the effect of these capsule strengths has not been studied in this age group.
Aprepitant Sandoz may affect the action of other medicines, both during and after treatment with aprepitant. Some medicines (such as pimozide, terfenadine, astemizole, and cisapride) should not be taken at the same time as Aprepitant Sandoz or may require dose adjustment (see also "When not to take Aprepitant Sandoz"). Taking Aprepitant Sandoz with other medicines, including those listed below, may affect the action of Aprepitant Sandoz or other medicines. Tell your doctor or pharmacist if you are taking any of the following medicines:
Tell your doctor about all medicines you are taking or have recently taken, as well as any medicines you plan to take.
This medicine should not be used during pregnancy unless it is absolutely necessary. If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a baby, ask your doctor for advice before taking this medicine. For information on contraception, see "Aprepitant Sandoz and other medicines". It is not known whether Aprepitant Sandoz passes into breast milk, so breastfeeding is not recommended during treatment with this medicine. It is important to tell your doctor if you are breastfeeding or planning to breastfeed before starting treatment.
Remember that Aprepitant Sandoz may cause dizziness and drowsiness in some people. If this happens, do not drive or ride a bike, or operate machinery or tools (see "Possible side effects").
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
Always take this medicine exactly as your doctor, pharmacist, or nurse has told you. If you are not sure, ask your doctor, pharmacist, or nurse. Aprepitant Sandoz is always taken with other medicines that prevent nausea and vomiting. After stopping Aprepitant Sandoz, your doctor may recommend continuing to take other medicines that prevent nausea and vomiting, including corticosteroids (such as dexamethasone) and 5HT3 antagonists (such as ondansetron). If you are unsure, ask your doctor, pharmacist, or nurse. The recommended dose is:
and
The medicine can be taken with or without food. Swallow the capsules whole with a drink of water.
Do not take more medicine than your doctor has prescribed. If you have taken more than the prescribed dose, contact your doctor immediately.
If you miss a dose, ask your doctor for advice. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, Aprepitant Sandoz can cause side effects, although not everybody gets them.
If you experience any side effects, including any not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301/fax: +48 22 49 21 309/website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date stated on the carton after EXP. The expiry date refers to the last day of that month. There are no special storage instructions for this medicine. Take the capsule out of the blister pack immediately before taking the medicine. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance is aprepitant. Aprepitant Sandoz, 80 mgEach hard capsule contains 80 mg of aprepitant. Aprepitant Sandoz, 125 mgEach hard capsule contains 125 mg of aprepitant. The other ingredients are sucrose, microcrystalline cellulose spheres 500, hydroxypropylcellulose, sodium lauryl sulfate, gelatin, titanium dioxide (E 171). The 125 mg capsules also contain iron oxide red (E 172).
Aprepitant Sandoz, 80 mgOpaque white capsules with a white body and white cap, containing white or almost white pellets. Aprepitant Sandoz, 125 mgOpaque white capsules with a white body and pink cap, containing white or almost white pellets. The medicine is available in a 3-day treatment pack, containing one blister with a 125 mg capsule and one blister with 80 mg capsules.
Sandoz GmbH Biochemiestrasse 10 6250 Kundl, Austria
Rontis Hellas Medical and Pharmaceutical Products S.A. P.O. Box 3012 Larissa Industrial Area 41 500 Larissa, Greece Lek Pharmaceuticals d.d. Verovškova ulica 57 1526 Ljubljana, Slovenia
Sandoz Polska Sp. z o.o. ul. Domaniewska 50 C 02-672 Warsaw tel. 22 209 70 00 Date of last revision of the leaflet:03/2024 Sandoz logo
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