Примери за използване на Intravenous or subcutaneous на Английски и техните преводи на Български
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For intravenous or subcutaneous use.
Post-operative pain: single intravenous or subcutaneous injection.
Intravenous or subcutaneous use.
Previous weekly epoetin intravenous or subcutaneous dose(IU/week).
Single intravenous or subcutaneous injection at a dosage of 0.2 mg meloxicam/ kg body weight i. e.
Post-operative pain: single intravenous or subcutaneous injection.
Patients currently treated with an ESA can be switched to MIRCERA administered once a month as a single intravenous or subcutaneous injection.
Monthly MIRCERA intravenous or subcutaneous dose(microgram/once monthly).
Method of administration Bortezomib SUN is available for intravenous or subcutaneous administration.
In no case should intravenous or subcutaneous injection be allowed.
Alternatively, a starting dose of 0.6 microgram/kg bodyweight may be administered once every two weeks as a single intravenous or subcutaneous injection in patients on dialysisor not on dialysis.
Daclizumab was well tolerated after single bolus intravenous or subcutaneous doses ranging from 50 to 125 mg/kg in mice, rats, and rabbits and after 28 days administration of 15 mg/kg to monkeys.
At the same timepoints, 88% and 79% of patients remained free from PAH worsening(defined as all-cause death, lung transplantation,atrial septostomy or start of intravenous or subcutaneous prostanoid treatment).
That Bortezomib Accord is to be given only by intravenous or subcutaneous injections; no other route of administration is allowed.
Nespo was as effective as human recombinant erythropoietin at increasing the haemoglobin levels in patients with kidney disease, and at keeping these levels maintained after they had been improved,whether given as an intravenous or subcutaneous injection.
MIRCERA starting doses Previous weekly darbepoetin alfa intravenous or subcutaneous dose(microgram/week).
Bortezomib SUN is administered via intravenous or subcutaneous injection at the recommended dose of 1.3 mg/m2 body surface area twice weekly for two weeks on days 1, 4, 8, and 11 in a 21-day treatment cycle.
It is important to check the product labels to ensure that the correct formulation(intravenous or subcutaneous) is being administered to the patient, as prescribed.
Bortezomib Accord is administered via intravenous or subcutaneous injection at the recommended dose of 1.3 mg/m2 body surface area twice weekly for two weeks on days 1, 4, 8, and 11 in a 28-day treatment cycle.
The recommended starting dose is 0.6 microgram/ kg body weight,administered once every two weeks as a single intravenous or subcutaneous injection in order to increase haemoglobin levelsto greater than 10 g/ dl(6.21 mmol/ l).
If any serious allergic or anaphylactic reaction occurs, intravenous or subcutaneous ORENCIA therapy should be discontinued immediately and appropriate therapy initiated, and the use of ORENCIA should be permanently discontinued.
The recommended starting dose of bortezomib is 1.3 mg/m2 intravenous or subcutaneous once daily, on the days shown in Table 1.
In animals at anaesthetic risk(e. g. aged animals) intravenous or subcutaneous fluid therapy during anaesthesia should be taken into consideration.
It is important to check the product labels to ensure that the correct formulation(intravenous or subcutaneous fixed dose) is being administered to the patient, as prescribed.
In animals at anaesthetic risk(e.g. aged animals) intravenous or subcutaneous fluid therapy during anaesthesia should be taken into consideration.
It is important to check the medicinal product labels to ensure that the appropriate formulation(intravenous or subcutaneous formulation) and strength is being given to the patient, as prescribed.
Reduction of post-operative pain(over a period of 24 hours):single intravenous or subcutaneous injection before surgery, for example at the time of induction of anaesthesia.
Reversible neutropenia was seen following daily intravenous or subcutaneous dosing for 30 days, but not following single doses or daily dosing for 14 days.
The primary target organs identified in the repeat-dose toxicology studies by parenteral routes(intravenous or subcutaneous) up to 1-year duration in mice and monkeys were the lymphoid and haematopoietic system.