Dasanix (Dasatinib) 50 MG – 30 Tablets

Description

Dasanix is an oral BCR-ABL tyrosine kinase inhibitor use to treat Chronic Myeloid Leukemiamia and Ph+ Acute Lymphoblastic Leukemia.

Product Features

Indications of Dasanix

It indicate for the treatment of adults with:
Newly diagnosed Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase.Chronic, accelerated, or myeloid or lymphoid blast phase Ph+ CML with resistance or intolerance to prior therapy including imatinib.Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy.

Pharmacology Dasatinib

Dasanix, at nanomolar concentrations, inhibits the following kinases: BCR-ABL, SRC family (SRC, LCK, YES, FYN), c-KIT, EPHA2, and PDGFRβ. Based on modeling studies, dasatinib predict to bind to multiple conformations of the ABL kinase. In vitro, Dasatinib was active in leukemic cell lines representing variants of imatinib mesylate sensitive and resistant disease. Dasatinib inhibited the growth of chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL) cell lines overexpressing BCR-ABL. Under the conditions of the assays, dasatinib was able to overcome imatinib resistance resulting from BCR-ABL kinase domain mutations, activation of alternate signaling pathways involving the SRC family kinases (LYN, HCK), and multi-drug resistance gene overexpression.

Dosage & Administration Dasatinib

The recommended starting dosage of Dasatinib for: Chronic phase CML is 100 mg administered orally once daily. Accelerated phase CML, myeloid or lymphoid blast phase CML, or Ph+ ALL is 140 mg administer orally once daily. Tablets not to crush or cut; they swallowed whole. Dasatinib need to taken with or without a meal, either in the morning or in the evening.

In clinical studies, treatment with Dasatinib continue until disease progression or until no longer tolerated by the patient. The effect of stopping treatment on long-term disease outcome after the achievement of a cytogenetic response (including complete cytogenetic response [CCyR]) or major molecular response (MMR) is not known.

Interaction

Concomitant use with drugs that have narrow therapeutic index (e.g. alfentanil, cisapride, ciclosporin, fentanyl, pimozide, quinidine, simvastatin, sirolimus, tacrolimus, ergot alkaloids) as it may increase the serum levels of these drugs. Increased risk of bleeding and thrombocytopenia with antiplatelet drugs, anticoagulants, and NSAIDs.

Contraindications

Concomitant use with CYP3A4 inhibitors (e.g. atazanavir, clarithromycin, erythromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin,  voriconazole or grapefruit juice); CYP3A4 inducers (e.g. carbamazepine, dexamethasone, phenytoin, phenobarbital, rifampicin or St John’s wort); antacid. Pregnancy.

Side Effects

Reversible myelosuppression, neutropenia, anaemia, thrombocytopenia, fluid retention, pulmonary arterial HTN, QT prolongation, cardiac failure, arrhythmias, HTN, musculoskeletal pain, GI disturbances, headache, chills, fatigue, asthenia, myalgia, chest pain, arthralgia, pyrexia, mucositis, flushing, colitis, electrolyte disturbances, appetite and wt disturbances, rash, dermatitis, hyperhidrosis, pruritus, acne.

Pregnancy & Lactation

Pregnancy category D. There is positive evidence of human fetal risk, but the benefits from use in pregnant women acceptable despite the risk (e.g., if the drugs need in a life-threatening situation or for a serious disease for which safer drugs cannot use or are ineffective).

Precautions & Warnings

Patients with predisposing factors for QT prolongation (e.g. congenital long QT syndrome, hypokalaemia, hypomagnesaemia, on antiarrhythmic therapy, or receiving cumulative high doses of anthracyclines). Hepatic impairment. Lactation.

Use in Special Populations

Pediatric Use: The safety and efficacy of Dasatinib in patients less than 18 years of age not to establish.

Geriatric Use: No differences in confirmed Complete Cytogenetic Response (cCCyR) and MMR observed between older and younger patients. Of the 2712 patients in clinical studies of Dasatinib, 617 (23%) were 65 years of age and older, and 123 (5%) were 75 years of age and older.

While the safety profile of Dasatinib in the geriatric population was similar to that in the younger population, patients aged 65 years and older are more likely to experience the commonly reported adverse reactions of fatigue, pleural effusion, diarrhea, dyspnea, cough, lower gastrointestinal hemorrhage, and appetite disturbance, and more likely to experience the less frequently reported adverse reactions of abdominal distention, dizziness, pericardial effusion, congestive heart failure, hypertension, pulmonary edema, and weight decrease, and should be monitored closely.

Hepatic Impairment: No dosage adjustment is necessary in patients with hepatic impairment. Caution recommended when administering Dasatinib to patients with hepatic impairment.

Renal Impairment: There are currently no clinical studies with Dasatinib in patients with impaired renal function. Less than 4% of dasatinib and its metabolites excreted via the kidney.

Delivery Country List:

United States, Canada, Mexico, Brazil, Argentina, United Kingdom, France, Germany, Italy, Spain, Portugal, Netherlands, Belgium, Switzerland, Austria, Sweden, Norway, Denmark, Finland, Iceland, Russia, China, Japan, South Korea, North Korea, Vietnam, Thailand, Malaysia, Singapore, Indonesia, Philippines, Australia, New Zealand, South Africa, Egypt, Nigeria, Kenya, Ethiopia, Morocco, Turkey, Saudi Arabia, United Arab Emirates, Iran, Iraq, Syria, Lebanon, Jordan, Qatar, Bahrain, Kuwait, Oman, Yemen, Afghanistan, Sri Lanka, Nepal, Bhutan, Maldives.

Myanmar, Cambodia, Laos, Mongolia, Kazakhstan, Uzbekistan, Turkmenistan, Kyrgyzstan, Tajikistan, Azerbaijan, Armenia, Georgia, Ukraine, Belarus, Poland, Czech Republic, Slovakia, Hungary, Romania, Bulgaria, Greece, Albania, Serbia, Montenegro, Bosnia and Herzegovina, Croatia, Slovenia, North Macedonia, Kosovo, Malta, Cyprus, Tunisia, Algeria, Libya, Sudan, Sierra Leone, Liberia, Ivory Coast, Ghana, Uganda, Zambia, Malawi, Zimbabwe, Namibia, Angola, Somalia, Eritrea. Etc…

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