{"id":2525,"date":"2026-04-20T11:37:20","date_gmt":"2026-04-20T11:37:20","guid":{"rendered":"https:\/\/emergencydrug.com\/?post_type=product&#038;p=2525"},"modified":"2026-04-21T06:14:42","modified_gmt":"2026-04-21T06:14:42","slug":"tucaxen-150-mg-tucatinib","status":"publish","type":"product","link":"https:\/\/emergencydrug.com\/ar\/shop\/tucaxen-150-mg-tucatinib\/","title":{"rendered":"Tucaxen 150 MG (Tucatinib) &#8211; 30 Tablets"},"content":{"rendered":"<h4 class=\"fs18 mt30 mb10 color\"><strong><em>Product Features of\u00a0 Tucaxen 150 mg:<\/em><\/strong><\/h4>\n<table width=\"322\">\n<tbody>\n<tr>\n<td>Product Name<\/td>\n<td>: <span data-preserver-spaces=\"true\">Tucaxen<\/span><\/td>\n<\/tr>\n<tr>\n<td>Generic Name<\/td>\n<td>: <span data-preserver-spaces=\"true\">Tucatinib<\/span><\/td>\n<\/tr>\n<tr>\n<td>Manufacturer<\/td>\n<td>: Everest Pharma Ltd<\/td>\n<\/tr>\n<tr>\n<td>Indication<\/td>\n<td>: Breast Cancer<\/td>\n<\/tr>\n<tr>\n<td>Formulation<\/td>\n<td>: Tablet<\/td>\n<\/tr>\n<tr>\n<td>Strength<\/td>\n<td>: 150 mg<\/td>\n<\/tr>\n<tr>\n<td>Quantity<\/td>\n<td>: 30 Tablets<\/td>\n<\/tr>\n<tr>\n<td>Storage<\/td>\n<td>: Below 30\u00b0<\/td>\n<\/tr>\n<tr>\n<td>Registrations<\/td>\n<td>: Export Only<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>Tucaxen 150 mg price:<\/strong> $550.00<\/p>\n<p>&nbsp;<\/p>\n<p><span data-preserver-spaces=\"true\">Tucaxen 150 Mg (Tucatinib), generic Tukysa, is used with trastuzumab (Herceptin) and capecitabine (Xeloda) to treat a certain type of hormone receptor-positive breast cancer that has spread to other parts of the body and cannot be treated with surgery in adults who have already been treated with at least one other chemotherapy medication. Tucatinib is in a class of drugs called kinase inhibitors. It works by blocking the action of the abnormal protein that signals cancer cells to multiply. This helps stop or slow the spread of cancer cells.<\/span><\/p>\n<p>&nbsp;<\/p>\n<h2 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">Composition<\/span><\/strong><\/h2>\n<p><strong><span data-preserver-spaces=\"true\">Tucaxen 50 Tablets<\/span><\/strong><span data-preserver-spaces=\"true\">: Each film-coated tablet contains Tucatinib INN 50 mg.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Tucaxen 150 Tablets<\/span><\/strong><span data-preserver-spaces=\"true\">: Each film-coated tablet contains Tucatinib INN 150 mg.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">Pharmacology\u00a0<\/span><\/strong><\/h3>\n<p><strong><span data-preserver-spaces=\"true\">\u00a0Mechanism of Action of\u00a0 Tucaxen 150 mg <\/span><\/strong><\/p>\n<p><span data-preserver-spaces=\"true\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Tucatinib\" target=\"_blank\" rel=\"noopener\">Tucatinib<\/a> is a tyrosine kinase inhibitor of HER2. In vitro, it inhibits phosphorylation of HER2 and HER3, resulting in inhibition of downstream MAPK and AKT signaling and cell proliferation, and showed anti-tumor activity in HER2 expressing tumor cells. In vivo, it inhibited the growth of HER2 expressing tumors. The combination of Tucatinib and trastuzumab showed increased anti-tumor activity in vitro and in vivo compared to either drug alone.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><strong><span data-preserver-spaces=\"true\">Pharmacodynamics<\/span><\/strong><\/p>\n<p><strong><span data-preserver-spaces=\"true\">\u00a0Exposure Response Relationship:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">Tucatinib exposure-response relationships and the time course of pharmacodynamics response have not been fully characterized.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Cardiac Electrophysiology:<\/span><\/strong> No large mean increase in QTc (i.e., &gt; 20 ms) was detected following treatment at the recommended dose of 300 mg taken orally twice daily.<\/p>\n<p><strong><span data-preserver-spaces=\"true\">Pharmacokinetics:<\/span><\/strong> Tucatinib AUCO-INF and Cmax increase proportionally over a dosage range from 50 mg to 300 mg (0.17 to 1 times the approved recommended dosage). Tucatinib exhibited 1.7-fold accumulation for AUC and 1.5-fold accumulation for Cmax after administering Tucatinib 300 mg twice daily for 14 days. The time to steady state was approximately 4 days.<\/p>\n<p><strong><span data-preserver-spaces=\"true\">Absorption:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">The median time to peak plasma concentration of Tucatinib was approximately 2 hours (range 1 to 4 hours).\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Effects of Food:<\/span><\/strong><\/p>\n<ul>\n<li>After administering<span data-preserver-spaces=\"true\">\u00a0a single oral dose of Tucatinib to 11 subjects after a high-fat meal (approximately 58% fat, 26% carbohydrate, and 16% protein), the mean AUCO-INF increased by 1.5-fold.<\/span><\/li>\n<li><span data-preserver-spaces=\"true\">The Tmax shifted from 1.5 hours to 4 hours.<\/span><\/li>\n<li><span data-preserver-spaces=\"true\">Cmax was unaltered.<\/span><\/li>\n<\/ul>\n<p><span data-preserver-spaces=\"true\">The effect of food on the pharmacokinetics of Tucatinib was not clinically meaningful.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Distribution:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">The geometric mean (CV%) apparent volume of distribution of Tucatinib was approximately 1670 L (66%). The plasma protein binding was 97.1% at clinically relevant concentrations.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Elimination:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">The geometric mean (CV%) half-life of Tucatinib was approximately 8.5 (21%) hours, and apparent clearance was 148 L<\/span><em><span data-preserver-spaces=\"true\">\/<\/span><\/em><span data-preserver-spaces=\"true\">h (55%).\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Metabolism:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">Tucatinib 150 mg is metabolized primarily by CYP2C8 and somewhat via CYP3A.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Excretion:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">Following a single oral dose of 300 mg radiolabeled Tucatinib, approximately 86% of the total radiolabeled dose was recovered in feces (16% of the administered dose as unchanged Tucatinib) and 4.1% in urine, with an o<\/span><em><span data-preserver-spaces=\"true\">v<\/span><\/em><span data-preserver-spaces=\"true\">erall total reco<\/span><em><span data-preserver-spaces=\"true\">v<\/span><\/em><span data-preserver-spaces=\"true\">ery of 90% within 13 days post-dose. Approximately 76% of the plasma radioactivity was unchanged, 19% was attributed to identified metabolites, and approximately 5% was unassigned.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">Indication of\u00a0 Tucaxen 150 mg Tablet<\/span><\/strong><\/h3>\n<p><span data-preserver-spaces=\"true\">Tucatinib 150 mg is combined with trastuzumab and capecitabine to treat adult patients with advanced unrespectable or metastatic HER2-positive breast cancer, including patients with brain metastases who have received one or more prior anti-HER2-based regimens in the metastatic setting.<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">DOSAGE AND ADMINISTRATION of\u00a0 Tucaxen 150 mg<\/span><\/strong><\/h3>\n<p><strong><span data-preserver-spaces=\"true\">Recommended Dosage:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">The recommended dosage is 300 mg, taken orally twice daily in combination with trastuzumab and capecitabine until disease progression or unacceptable toxicity.<\/span><\/p>\n<p>The tablets should be swallowed whole, not chewed, crushed, or split. It would be best if you never consumed a tablet that is broken, cracked, or otherwise non-intact. Each dose should be taken approximately 12 hours apart and simultaneously with or without a meal daily.<\/p>\n<p><span data-preserver-spaces=\"true\">If the patient vomits or misses a dose, the patient is advised to take the following amount at its usual scheduled time.<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">When given in combination with Tucatinib, the recommended dosage of capecitabine is 1000 mg\/m2 orally twice daily, taken within 30 minutes after a meal. Tucatinib and capecitabine can be taken at the same time.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><strong><span data-preserver-spaces=\"true\">Dosage Modifications for Adverse Reactions of Tucaxen 150 mg<\/span><\/strong><\/p>\n<p><strong><span data-preserver-spaces=\"true\">\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">Recommended Dose Reductions for Adverse Reactions. Permanently discontinue Tucatinib in patients unable to tolerate 150 mg orally twice daily.<\/span><\/p>\n<p><img data-recalc-dims=\"1\" decoding=\"async\" class=\"alignnone size-full wp-image-2560\" src=\"https:\/\/i0.wp.com\/emergencydrug.com\/wp-content\/uploads\/2022\/09\/Dosage-Modifications-for-Adverse-Reactions-1.png?resize=381%2C110&#038;ssl=1\" alt=\"\" width=\"381\" height=\"110\" title=\"\" srcset=\"https:\/\/i0.wp.com\/emergencydrug.com\/ar\/wp-content\/uploads\/2022\/09\/Dosage-Modifications-for-Adverse-Reactions-1.png?w=381&amp;ssl=1 381w, https:\/\/i0.wp.com\/emergencydrug.com\/ar\/wp-content\/uploads\/2022\/09\/Dosage-Modifications-for-Adverse-Reactions-1.png?resize=300%2C87&amp;ssl=1 300w\" sizes=\"(max-width: 381px) 100vw, 381px\" \/><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Dosage Modifications for Severe Hepatic Impairment<\/span><\/strong><\/p>\n<p>F<span data-preserver-spaces=\"true\">or patients with severe hepatic impairment (Child-Pugh C) reduce the recommended dosage to 200 mg orally twice daily.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><strong><span data-preserver-spaces=\"true\">\u00a0Dosage Modifications for Concomitant Use with Strong CYP2C8 Inhibitors\u00a0<\/span><\/strong><\/p>\n<p><span data-preserver-spaces=\"true\">Avoid concomitant use of strong CYP2C8 inhibitors with Tucatinib. If concomitant use with a strong CYP2C8 inhibitor cannot be avoided, reduce the recommended dosage to 100 mg orally twice daily. After discontinuing the strong CYP2C8 inhibitor for 3 elimination half-lives, resume the dose taken before initiating the inhibitor.<\/span><\/p>\n<h3><\/h3>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">CONTRAINDICATION<\/span><\/strong><\/h3>\n<p style=\"text-align: left;\"><span data-preserver-spaces=\"true\">None.<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">WARNING AND PRECAUTION\u00a0<\/span><\/strong><\/h3>\n<p><strong><span data-preserver-spaces=\"true\">Diarrhea:\u00a0<\/span><\/strong><span data-preserver-spaces=\"true\">Tucatinib 150 mg can cause severe diarrhea, dehydration, hypotension, acute kidney injury, and death. In HER2CLIMB, 81% of patients who received this experienced diarrhea, including 12% with Grade 3 diarrhea and 0.5% with Grade 4 diarrhea. Both patients who developed Grade 4 diarrhea subsequently died, with diarrhea contributing to death. The median time to onset of the first episode of diarrhea was 12 days and the median time to resolution was 8 days. Diarrhea led to dose reductions in 6% of patients and discontinuation in 1% of patients. Prophylactic use of antidiarrheal treatment was not required on HER2CLIMB.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">If diarrhea occurs, administer antidiarrheal treatment as clinically indicated. Perform diagnostic tests as clinically indicated to exclude other causes of diarrhea. Based on the severity of diarrhea, interrupt the dose, then reduce the dose or permanently discontinue the dose.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Hepatotoxicity:<\/span><\/strong><span data-preserver-spaces=\"true\"> Tucatinib 150 mg can cause severe hepatotoxicity. In HER2CLIMB, 8% of patients who received had an ALT increase &gt; 5 x ULN, 6% had an AST increase &gt; 5 x ULN, and 1.5% had a bilirubin increase &gt; 3 x ULN (Grade 23). Hepatotoxicity led to dose reduction in 8% of patients and discontinuation in 1.5% of patients.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">Monitor ALT, AST, and bilirubin before starting Tucatinib, every 3 weeks during treatment, and as clinically indicated. Based on the severity of hepatotoxicity, interrupt the dose, then reduce the dose or permanently discontinue the dose.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Embryo-Fetal Toxicity:<\/span><\/strong><\/p>\n<p><span data-preserver-spaces=\"true\">Based on animal studies and its mechanism of action, it can cause fetal harm when administered to a pregnant woman. In animal reproduction studies, administration to pregnant rats and rabbits during organogenesis caused embryo-fetal mortality, reduced fetal weight and fetal abnormalities at maternal exposures &gt; 1.3 times the human exposure\u00a0<\/span><em><span data-preserver-spaces=\"true\">(<\/span><\/em><span data-preserver-spaces=\"true\">AUC) at the recommended dose.\u00a0<\/span><\/p>\n<p>Pregnant women and females with reproductive potential should be informed of the potential risk to their fetuses. Use effective contraception during treatment with Tucatinib and for at least one week after the last dose if you are a female with reproductive potential. Men with female partners of reproductive potential should use effective contraception during and after treatment with Tucatinib.<\/p>\n<p>It is used in combination with trastuzumab and capecitabine.<\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">Tucaxen 150 MG Side Effects<\/span><\/strong><\/h3>\n<p><span data-preserver-spaces=\"true\">The following clinically significant side effects are observed:\u00a0<\/span><\/p>\n<ul>\n<li><span data-preserver-spaces=\"true\">Diarrhea\u00a0<\/span><\/li>\n<li><span data-preserver-spaces=\"true\">Hepatotoxicity\u00a0<\/span><\/li>\n<\/ul>\n<p><span data-preserver-spaces=\"true\">The most common side effects in patients (20%) were diarrhea, palmar-plantar Erythrodysesthesia, nausea, fatigue, hepatotoxicity, vomiting, stomatitis, decreased appetite, abdominal pain, headache, anemia, and rash.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">USE IN SPECIFIC POPULATIONS<\/span><\/strong><\/h3>\n<p><strong><span data-preserver-spaces=\"true\">\u00a0Pregnancy\u00a0<\/span><\/strong><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Risk Summary:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Tucatinib is used in combination with trastuzumab and capecitabine.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">Specific Populations Age (&lt; 65 (n =211); &gt; 65 (n = 27)), albumin (25 to 52 g\/L), creatinine clearance (creatinine clearance [CLcr] 60 to 89 mL\/min (n = 89); CLcr 30 to 59 mL\/min (n = 5)), body weight (41 to 138 kg), and race (White (n=168), Black (n=53), or Asian (n=10)) did not have a clinically meaningful effect on Tucatinib exposure.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">Based on animal findings and its mechanism of action, Tucatinib can cause fetal harm when administered to a pregnant woman. There are no available human data on Tucatinib use in pregnant women to inform a drug-associated risk. Advise pregnant women and females of reproductive potential of the potential risk to the fetus.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">The background risk of major congenital disabilities and miscarriage for the indicated population is unknown.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><strong><span data-preserver-spaces=\"true\">Lactation\u00a0<\/span><\/strong><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Risk Summary:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Tucatinib is used in the capecitabine combination.<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">There is no data on the presence of Tucatinib, its metabolites in human or animal milk, or its effects on the breastfed child or milk production. Because of the potential for serious adverse reactions in a breastfed child, advise women not to breastfeed during treatment with Tucatinib and for at least 1 week after the last dose.\u00a0<\/span><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Females and Males of Reproductive Potential:<\/strong> <\/span><\/em>Tucatinib can cause fetal harm when administered to a pregnant woman Tucatinib is used in combination with trastuzumab and capecitabine.<\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Pregnancy Testing:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Verifies the pregnancy status of females of reproductive potential before initiating treatment with Tucatinib.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Contraception<\/span><\/strong><\/p>\n<p><strong>\u00a0<em>Females: <\/em><\/strong>During and after treatment with Tucatinib, females of reproductive potential should use effective contraception.<\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Males:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Male patients with female partners of reproductive potential are advised to use effective contraception during treatment with Tucatinib and for at least 1 week after the last dose.\u00a0<\/span><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Infertility:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Based on findings from animal studies, Tucatinib may impair male and female fertility.\u00a0<\/span><\/p>\n<p><strong><em>Pediatric U<\/em>s<em>e:\u00a0<\/em><\/strong><span data-preserver-spaces=\"true\">The safety and effectiveness of Tucatinib in pediatric patients have not been established.\u00a0<\/span><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Geriatric Use:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">In HER2CLIMB, 82 patients who received Tucatinib were &gt; 65 years, of whom 8 were &gt;\u00a0<\/span><em><span data-preserver-spaces=\"true\">7<\/span><\/em><span data-preserver-spaces=\"true\">5 years old. The incidence of serious adverse reactions in those receiving Tucatinib was 34% in patients 2 65 years compared to 24% in patients &lt;65 years. The most frequent serious adverse reactions in patients who received Tucatinib and 2 65 years were diarrhea (9%), vomiting (6%), and nausea (5%). There were no observed overall differences in the effectiveness of Tucatinib in patients &gt; 65 years compared to younger patients. There were too few patients at 275 years to assess differences in effectiveness or safety.\u00a0<\/span><\/p>\n<p><em><span data-preserver-spaces=\"true\"><strong>Renal Impairment:<\/strong>\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Tucatinib, in combination with capecitabine and trastuzumab, is not recommended in patients with severe renal impairment (CLcr &lt; 30 mL<\/span><em><span data-preserver-spaces=\"true\">\/m<\/span><\/em><span data-preserver-spaces=\"true\">in estimated by Cockcroft-Gault Equation) because capecitabine is contraindicated in patients with severe renal impairment.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">No dose adjustment is recommended for patients with mild or moderate renal impairment (creatinine clearance [CLcr] 30 to 89 mL\/min).\u00a0<\/span><\/p>\n<p><strong><em>Hepatic Impairment:\u00a0<\/em><\/strong><span data-preserver-spaces=\"true\">Tucatinib exposure is increased in patients with severe hepatic impairment (Child-Pugh C). Reduce the dose for patients with severe (Child-Pugh C) hepatic impairment.\u00a0<\/span><\/p>\n<p><span data-preserver-spaces=\"true\">No dose adjustment is required for patients with mild (Child-Pugh A) or moderate (Child-Pugh B) hepatic impairment.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">Overdose of Tucaxen 150 mg<\/span><\/strong><\/h3>\n<p><span data-preserver-spaces=\"true\">There is no specific antidote, and hemodialysis&#8217;s benefit in treating Tucatinib overdose is unknown. The treatment should be withheld in case of an overdose and should take general supportive measures.<\/span><\/p>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: left;\"><strong><span data-preserver-spaces=\"true\">PHARMACEUTICAL INFORMATION\u00a0<\/span><\/strong><\/h3>\n<p><strong><span data-preserver-spaces=\"true\">Storage\u00a0<\/span><\/strong><\/p>\n<p><span data-preserver-spaces=\"true\">Store below 25\u00b0C, in a cool and dry place. Keep away from light. Keep out of the reach of children.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">How To Supply?<\/span><\/strong><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Tucaxen 50 tablet:<\/span><\/strong><span data-preserver-spaces=\"true\">\u00a0Each HDPE container contains 30 film-coated tablets (each tablet contains 50 mg Tucatinib), a silica gel desiccant and a polyester coil with a child-resistant closure.\u00a0<\/span><\/p>\n<p><em><span data-preserver-spaces=\"true\">Males\u00a0<\/span><\/em><span data-preserver-spaces=\"true\">Male patients with female partners of reproductive potential are advised to use effective contraception during treatment with Tucatinib and for at least 1 week after the last dose.\u00a0<\/span><\/p>\n<p><strong><span data-preserver-spaces=\"true\">Tucaxen 150 tablet:<\/span><\/strong><span data-preserver-spaces=\"true\">\u00a0Each HDPE container contains 30 film-coated tablets (each tablet contains 150 mg Tucatinib), a silica gel desiccant and a polyester coil with a child-resistant closure.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>To see more oncology medicine <a href=\"https:\/\/emergencydrug.com\/shop\"><span style=\"color: #ff0000;\"><strong>CLICK HERE<\/strong><\/span><\/a><\/p>\n<p><span data-preserver-spaces=\"true\">\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p><span data-preserver-spaces=\"true\">Tucaxen 150 mg (Tucatinib), generic Tukysa, is used with trastuzumab (Herceptin) and capecitabine (Xeloda) to treat a certain type of hormone receptor-positive breast cancer that has spread to other parts of the body and cannot be treated with surgery in adults who have already been treated with at least one other chemotherapy medication. Tucatinib is in a class of drugs called kinase inhibitors. It works by blocking the action of the abnormal protein that signals cancer cells to multiply. This helps stop or slow the spread of cancer cells.<\/span><\/p>\n","protected":false},"featured_media":3070,"comment_status":"open","ping_status":"closed","template":"","meta":[],"mc_generic":[411],"brands":[404],"product_cat":[434,108],"product_tag":[585,583,582,586,584,580,579,581],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/product\/2525"}],"collection":[{"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/comments?post=2525"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/media\/3070"}],"wp:attachment":[{"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/media?parent=2525"}],"wp:term":[{"taxonomy":"mc_generic","embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/mc_generic?post=2525"},{"taxonomy":"brands","embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/brands?post=2525"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/product_cat?post=2525"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/emergencydrug.com\/ar\/wp-json\/wp\/v2\/product_tag?post=2525"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}