Showing 13–24 of 201 results

  • pulmonary hypertension

    Tadalafil

    【Product name】Cialis

    [English common name]Tadalafil

    [Chinese common name]Tadanafil

    [English name]IC-351

    [Chinese other name]Hedi

    [indications] erectile dysfunction andpulmonary hypertension.

    [Usage and Dosage] The recommended dose of this product is 10mg. It is taken before sexual life and is not affected by eating. If the effect of taking 10mg is not significant, you can take 20mg. It can be taken at least 30 minutes before sex. The maximum frequency of medication is Once a day.

    [Storage] Store at room temperature.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • 血小板减少症

    Equippa

    【Product name】Promacta

    [English common name]Equippa

    [Chinese common name]Equippa

    [English name]

    [Chinese other name]

    [Indications] Chronic immunity (idiopathic) in adults and pediatric patients over 1 year old Thrombocytopenia (ITP)

    [Usage and Dosage] Fasting (1 hour or 2 hours after a meal), daily adult and pediatric patients over 6 years old start PROMACTA 50 mg daily, 25 mg per day for pediatric patients between 1 and 5 years old. Patients with liver damage and patients of East Asian descent require a dose reduction. Adjust to maintain a platelet count greater than or equal to 50 x 10 9 / liter. Do not exceed 75 mg per day.

    [Storage] Store at room temperature between 20 ° C and 25 ° C (68 ° F to 77 ° F); allow tours to 30 ° C (59 ° F to 86 ° F). Do not remove desiccant if present. Exempt the original bottle.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Breast cancer

    Ixapilone

    【Product name】Ixempra

    [English common name]Ixabepilone

    [Chinese common name]Ixapilone

    [English name]Ipsapironum

    [Chinese other name]1-dioxide

    [Indications] IXEMPRA combined with capecitabine for the treatment of metastatic or local advancedBreast cancerPatients who are resistant to anthracyclines and taxanes, or whose cancers have taxane resistance and are further contraindicated for their anthracycline treatment. Anthracycline resistance is defined as the progressive metastatic environment during treatment or within 6 months or within 3 months of the adjuvant treatment group. Taxane resistance is defined as progression at treatment or within 12 months of adjuvant therapy or at 4 months in a metastatic environment.
    IXEMPRA is indicated for the treatment of advanced breast cancer anthracyclines, taxanes and capecitabine in patients with metastatic or local monotherapy tumor-resistant or refractory patients.

    [Usage and Dosage] The recommended dose of IXEMPRA is 40 mg / m 2 and intravenous administration for 3 hours every 3 weeks. The dose of a patient with a body surface area (BSA) greater than 2.2 m2 should be calculated according to 2.2 m2.

    [Storage] The IXEMPRA kit must be stored in a refrigerator at 2 ° C to 8 ° C (36 ° F to 46 ° F). Keep the original packaging until it is used to prevent light.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Osteoporosis in postmenopausal women

    Ibandan sodium

    [product name] BONIVA

    [English common name]Ibandronate

    [Chinese common name]Ibandronate injection

    [English name]

    [Chinese other name]

    [Indications] BONIVA is suitable for treatment and preventionOsteoporosis in postmenopausal women.

    [Usage and Dosage] The recommended dose of BONIVA for the treatment and prevention of postmenopausal osteoporosis is a 2.5 mg film-coated tablet once a day.

    [Storage] Store BONIVA at 77 °F (25 °C) or room temperature between 59 °C and 86 °F (15 °C and 30 °C).

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Chronic myeloid leukemia , scleroderma

    Imatinib

    【Product name】Imatinib

    [English common name]GLEEVEC

    [Chinese common name]Imatinib

    [English name]Imatinib intermediates, imatinib

    [Chinese other name]Imatinib intermediate, imatinib

    [indications]
    Imatinib mesylate capsule: for treatmentChronic myeloid leukemia(CML) chronic phase, accelerated phase, or chronic phase after failure of alpha-interferon therapy; malignancy that cannot be surgically removed or metastasizedGastrointestinal stromal tumor (GIST)patient.
    Imatinib mesylate tablets: for the treatment of chronic chromosome patients with chronic myeloid leukemia (CML) in Philadelphia, in the blast phase, accelerated phase, or chronic phase after failure of alpha-interferon therapy.
    Adult patients for the treatment of malignant gastrointestinal stromal tumors (GIST) that cannot be removed and/or metastasized.

    【Dosage】
    Imatinib mesylate capsule: starting dose: for patients with blast crisis and accelerated phase of chronic myeloid leukemia, the recommended dose of imatinib mesylate is 600 mg/day; for chronic patients who have failed interferon therapy, and For patients with malignant gastrointestinal stromal tumors (GIST) who cannot be surgically removed or metastasized, the recommended dose is 400 mg/day, which is taken once a day. It is advisable to take the medicine at mealtime and drink a large glass of water. It should be taken continuously.
    If the blood picture permits, there is no serious adverse drug reaction, the dose can be considered to increase from 400mg / day to 600mg / day, or from 600mg / day to 800mg / day (400mg, divided into 2 times) in the following cases: disease progression, treatment A satisfactory hematologic response was not obtained after at least 3 months, and the hematologic response that had been obtained disappeared again.
    The dose must be adjusted in the following cases: if a serious non-hematologic adverse reaction (such as severe water retention) occurs during the treatment, the drug should be discontinued until the adverse reaction disappears, and then the dose is adjusted according to the severity of the adverse reaction.
    Dose adjustment in severe liver toxicity: If the bilirubin rises more than 3 times the upper limit of the normal range or the transaminase rises more than 5 times the upper limit of the normal range, the drug should be discontinued until the above indicators fall to 1.5 or 2.5 times the upper limit of the normal range. the following.
    Adjustment of dose during neutropenia or thrombocytopenia: accelerated or blast phase: if severe neutrophils and thrombocytopenia occur (neutrophils <0.5×109/L and/or platelets<10×109/L The recommended dose is reduced to 400 mg / day. If the blood cells continue to decrease for 2 weeks, further reduce the dose to 300 mg / day, if the blood cells continue to decrease for 4 weeks, it is advisable to stop the drug until neutrophils ≥ (greater than or equal to ) 1.0 × 109 / L and platelets ≥ (greater than or equal to) 20 × 109 / L. When used again, the dose is 300 mg / day.
    Patients with chronic phase after failure of α-interferon therapy: neutrophils <1.0×109/L and/or platelets <50×109/L should be discontinued, only in granulocyte ≥ (greater than or equal to) 1.5 When x109/L and platelet ≥ (greater than or equal to) 75×109/L, the dosage is 400 mg/day. If the neutrophils or platelets are reduced to the above values, the dosage will be restored. Reduced to 300 mg / day.
    Children and adolescents: There are no clinical data on the safety and efficacy of imatinib mesylate in patients under 18 years of age.
    Dosage in patients with liver failure: The plasma concentration of imatinib mesylate can be increased in patients with liver damage, so these patients should be cautious when using this drug. There is no liver damage in patients with liver damage. Nie's clinical data, no suggestion for dose adjustment.
    Renal failure and dose in elderly patients: creatinine clearance is known to decrease with age, and age has no significant effect on the pharmacokinetics of imatinib mesylate, as it has not been performed in patients with impaired renal function. Clinical trials, so it is not possible to propose a dose adjustment.
    Imatinib mesylate tablets: starting dose: The initial treatment should be performed by a physician with experience in treating chronic myelogenous leukemia or GIST.
    The product should be taken orally, and it is advisable to take the medicine while eating and drink a large glass of water. Usually adults once a day. Children and adolescents take it once or twice a day (morning and evening).
    Patients (children) who cannot swallow tablets can disperse the tablets in water or apple juice. It is recommended that pregnant and lactating women avoid contact with skin or eyes when inhaling capsules, or inhalation (see pregnant and lactating women), and wash hands immediately after touching open capsules.
    - therapeutic dose of CML patients
    adult
    The recommended dose for patients in the chronic phase is 400 mg/day, and for the blast phase and accelerated phase, it is 600 mg/day.
    As long as it is effective, it should be taken continuously.
    If the blood picture permits, there is no serious adverse drug reaction, the dose can be considered to increase from 400 mg / day to 600 mg / day, or from 600 mg / day to 800 mg / day (400 mg, orally, 2 times) Taking): The disease has not been able to obtain a satisfactory hematologic response after at least 3 months of treatment, and the hematological response has disappeared.
    Children and adolescents over 3 years old
    So far, children have limited experience in medication. According to the adult dose, the recommended daily dose is: chronic phase 260mg / m2 (maximum dose: 400mg), accelerated phase and blast phase 340mg / m2 (maximum dose: 600mg), the daily recommended dose for children, the calculated dose is generally Should be close to or around 100mg, the dose for children under 12 should generally be as close as possible or around 50mg. There is no experience in treating children under 3 years of age.
    - therapeutic dose of GIST patients
    For patients with malignant GIST who cannot be removed and/or metastasized, the recommended dose for this product is 400 mg/day.
    A satisfactory response was not obtained after treatment. If there were no adverse drug reactions, the dose could be considered to increase from 400 mg/day to 600 mg/day. Treatment time:
    For patients with GIST, the product should be treated continuously unless the condition progresses.

    [Storage]
    Imatinib mesylate capsule: should be kept below 30 °C.
    Imatinib mesylate tablets should be kept below 30 °C.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Dermal T-cell lymphoma

    Vorino

    【Product name】Zolinza

    [English common name]Vorinostat

    [Chinese common name]Vorino

    [English name]

    [Chinese other name]

    [indications]Dermal T-cell lymphoma

    [Usage and Dosage] Adult: Oral once a day, 400 mg each time after meals. In addition, it is also necessary to apply according to the patient's condition.

    [Storage] Store at 20-25 ° C (68-77 ° F), and allow 15-30 ° C (59-86 ° F).

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Crohn's disease , Psoriatic arthritis (PsA)

    Utec monoclonal antibody

    【Product name】Stelara

    [English common name]Ustekinumab

    [Chinese common name]Utec monoclonal antibody

    [English name]

    [Chinese other name]

    [Indications] Stelara is a drug used to treat the following diseases:
    Moderate to severe plaque psoriasis (a disease that causes red, scaly plaque in the skin). It is used in adults and children over the age of 12, and its condition is unresponsive or cannot be treated with other systemic (systemic) psoriasis, such as cyclosporine, methotrexate or PUVA (psoralen UV A). PUVA is a treatment in which a patient receives a drug containing a compound called "psoralen" prior to exposure to ultraviolet light.
    Activity in adultsPsoriatic arthritis(Inflammation of the joints associated with psoriasis), when the condition is not adequately responsive to other treatments, is called anti-rheumatic drugs (DMARDs) that improve the disease. Stelara can be used alone or in combination with methotrexate (DMARD); moderate to severe activity in adultsCrohn's disease(a disease that causes intestinal inflammation), whose condition is poorly responsive to other Crohn's disease treatments or is unacceptable for such treatment.

    [Usage and Dosage] Adults aged 18 years and older started treatment with a loading dose of 320 mg delivered to two 2 ml, subcutaneously 160 mg on the same day at two different locations. Continue to use a weekly injection of 160 mg as a single, 2 ml, subcutaneously administered dose. Don't give ARCALYST more often than once a week. Pediatric patients are 12 to 17 years old: the starting dose for treatment is 4.4 mg/kg, up to 320 mg, delivered with one or two subcutaneous injections, with a maximum single injection volume of 2 mL. Continue to administer a weekly injection of 2.2 mg/kg, up to 160 mg, as a single subcutaneous injection, up to 2 ml. If the initial dose given is two injections, they should be on the same day at two different locations. Don't give ARCALYST more often than once a week.

    [Storage] Store in the refrigerator (2 ° C – 8 ° C). Do not freeze. Keep the vial in an outer carton to prevent light from shining.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Cystic fibrosis (CF)

    Ivacato

    [product name] Orkambi, Kalydeco

    [English common name] Ivacaftor

    [Chinese common name] Ivacakato

    [English name] Ivacaftor-D4

    [Other names in Chinese] quinoline formamide, ivacato

    [Indications] KALYDECO is classified as a cystic fibrosis transmembrane conductance regulator (CFTR) Synergist. KALYDECOSuitable for treatmentCFTRHave in the geneG551DMutation6Cystic fibrosis in patients aged one year and older (CF). If the patient's genotype is unknown, use itFDAApprovedCFMutation detection to detectG551DThe presence of a mutation.

    [Usage and Dosage] The recommended KALYDECO dose for adult and child patients aged 6 years and older is 150 mg tablets per 12 hours (300 mg daily total) and fat-containing foods. Examples of suitable fat-containing foods include eggs, butter, peanut butter, cheese pizza, and the like.

    [Storage] stored in20-25oC(68-77oF);Allow offset15-30oC(59-86oF)

    【Tips】Part of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctor's face diagnosis. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Coronary artery dilatation , Coronary artery occlusion

    Epeptide

    【Product name】Eptifibatide

    [English common name]Integrilin

    [Chinese common name] Epeptide

    [English name]

    [Chinese other name]

    [indications]For acuteCoronary syndromePatient treatment (notStable angina/Non-ST-segment elevation myocardial infarction):
    1. Patients who will receive medical treatment and patients undergoing percutaneous coronary intervention (PCI).
    2. Patients undergoing PCI, including those undergoing coronary stenting.

    【Dosage】The safety and efficacy of eptifibatide has been established in clinical studies in combination with heparin and aspirin. Different dosing regimens have been used for eptifibatide in clinical studies.
    Acute coronary syndrome
    (1) For patients with acute coronary syndrome and normal renal function, the recommended adult dose for this product is: 180 μg/kg intravenous bolus as soon as possible after diagnosis, followed by continuous vein at 2.0 μg/kg/min Instillation for 72 hours unless the patient is discharged or begins coronary artery bypass surgery (CABG). If the patient is undergoing percutaneous coronary intervention (PCI) during the course of receiving eptifibatide, the intravenous infusion will continue until the patient is discharged, or until 18-24 hours after treatment, the first occurrence in both cases, The treatment reached 96 hours.
    (2) For patients with acute coronary syndrome who have an estimated creatinine clearance (using the Cockroft-Gault formula) 2.0 mg/dL, the recommended adult dose is an intravenous bolus of 180 μg/kg as soon as possible after diagnosis. Immediately followed by a continuous intravenous drip of 1.0 μg/kg/min.
    2. Percutaneous coronary intervention (PCI)
    (1) For patients with normal renal function, the recommended adult dose of eptifibatide is 180 μg/kg intravenously before the start of PCI, followed by a continuous infusion of 2.0 μg/kg/min, and the first push A second bolus of 180 μg/kg was given 10 min after the injection. Intravenous infusion is required until the patient is discharged, or 18-24 hours after treatment, which occurs first in both cases. The infusion time is recommended for at least 12 hours.
    (2) For patients with estimated creatinine clearance (using the Cockroft-Gault formula) 2.0 mg/dL, the recommended adult dose is 180 μg/kg intravenously before the start of PCI, immediately following 1.0 μg/kg/min. A continuous instillation was given and a second bolus of 180 μg/kg was given 10 min after the first bolus.
    (3) For patients undergoing coronary artery bypass graft surgery, infusion of eptifibatide should be stopped prior to surgery.

    [Storage] Sealed and placed in a cool place.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Mantle cell lymphoma

    Ibrutinib

    【Product name】Imbruvica

    [English common name]Ibrutinib

    [Chinese common name]Ibrutinib

    [English name]Ibrutinib N-2, Ibrutinib intermeidate N-2, Ibrutinib INT1

    [Chinese other name]Ibbutinib intermediate N-2, Ibrutinib intermediate, Ibrutinib intermediate N-2

    [Indications] IMBRUVICA is a kinase inhibitor shown for the treatment of patients:
    Who received at least one pre-treatmentMantle cell lymphoma (MCL).
    Accelerate the approval of the overall response rate based on this indicator. This instruction continues to approve the clinical effectiveness validation team without a confirmatory trial.
    Chronic lymphocytic leukemia (CLL).
    Chronic lymphocyte leukemia17p is missing.
    Waldenstrom's macroglobulinemia (WM).

    [Usage and Dosage] MCL: 560 mg, once a day orally (4 capsules of 140 mg once daily).
    CLL and WM: 420 mg once daily (third grade 140 mg capsule once daily).
    Capsules should be taken orally in a glass of water. Do not open, rest, or chew capsules.

    [Storage] Bottles are stored at room temperature between 20 ° C and 25 ° C (68 ° F to 77 ° F). The tour is allowed between 15 ° C and 30 ° C (59 ° F to 86 ° F). Keep the original packaging until dispensing.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Non-small cell lung cancer (NSCLC)

    Crizotiny

    【Product name】XALKORI

    [English common name]Crizotinib

    [Chinese common name]Crizotiny

    [English name]Crizotinib

    [Chinese other name]Crizotinib

    [Indications] XALKORI is a kinase inhibitor suitable for the treatment of the following patients:
    (1) TransferNon-small cell lung cancer (NSCLC)Tumors were tested for anaplastic lymphoma kinase (ALK)-positive using an FDA-approved test.
    (2) Metastatic NSCLC whose tumor is ROS1-positive.

    【Dosage】
    (1) Recommended dose: 250 mg orally, 2 times a day.
    (2) Kidney damage: 250 mg orally, once a day in patients with severe renal impairment (creatinine clearance <30 mL / min) without dialysis.

    [Storage]Pfizer Lab:20-25 ° C (may vary by 15-30 ° C).

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

  • Coronary heart disease , Liver Disease

    Perfluoropropane lipid microspheres

    【Product name】Definity

    [English common name]Perflutren

    [Chinese common name]Perfluoropropane

    [English name]Perfluoropropane, Octafluoropropane, Perfluoropropaneminimum

    [Chinese other name]Octafluoropropane, perfluoropropane lipid microsphere suspension injection

    [indications]For the improvement of conventional echocardiography, the recognition of the left ventricular endocardial border is enhanced.

    【Dosage】Peripherally intravenous injection, the recommended dose is 0.01ml / kg each time.
    (1) Preparation of the drug: After the appearance of the test is qualified, the drug is mixed, and the force is not shaken to prevent the microsphere from rupturing and foaming. In order to keep the pressure constant so as not to break the microspheres, another injection needle should be inserted into the vial plug to pass the atmosphere to keep the pressure constant, and then the suspension is sucked into the syringe.
    (2) Drug injection: The patient takes the left lateral position (for echocardiography), and inserts the hair needle with the tee into the dorsal vein of the right upper limb or the median vein of the elbow. Use a 10 ml syringe to extract 10 ml of 0.9% sodium chloride injection to the end of the tee, and use a 1 ml or 2 ml syringe to extract the mixed perfluoropropane human albumin microsphere injection to the other end of the tee to about 1 ml/sec. The injection speed bolus, then with a 0.9% sodium chloride injection 5 ~ 10ml bolus to make the contrast agent in the tube all into the blood circulation, complete the ultrasound examination during the injection process. If the effect is not satisfactory, the injection dose can be increased to 0.02ml/kg for injection, but the total number of injections should not exceed 2 times.
    note:
    (1) Do not inject air into the bottle.
    (2) This product is required to reach room temperature before use.
    (3) If the appearance is unqualified and the rubber stopper is damaged, please do not use it; use it immediately after opening; if the product is fully mixed, the solution is clear and not evenly white, indicating that the microsphere may have been destroyed. Will cause the ultrasound contrast effect to be poor or disappear, please do not use; if the drug has foreign matter or precipitate, do not use. The time interval between mixing the liquid and refraction should not exceed 1 minute. If it is more than 1 minute, invert the syringe and gently rotate to mix the microspheres. A pillow of size 20 or larger should be inserted into the peripheral vein before injection. Do not use a syringe to draw blood before injecting this product to avoid clot formation in the syringe.

    [Storage]Refrigerate and store at 2-8 °C in the dark. Do not invert and shake vigorously. Freezing is strictly prohibited.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.