Examples of using Subcutaneous formulation in English and their translations into Portuguese
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Ecclesiastic
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Computer
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During the treatment course with Herceptin subcutaneous formulation in administration system,
During the treatment course with Herceptin subcutaneous formulation other medicinal products for subcutaneous administration should preferably be injected at different sites.
Of patients treated with Herceptin subcutaneous formulation developed antibodies against the excipient hyaluronidase rHuPH20.
Local cutaneous reactions including injection site reactions were very common in patients receiving MabThera subcutaneous formulation.
Administration related reactions have been observed in up to 50% of patients treated with MabThera subcutaneous formulation in clinical trials.
severe infections(NCI CTCAE grade≥3) was 5.0% versus 7.1%, in the Herceptin intravenous formulation arm and the Herceptin subcutaneous formulation arm respectively.
were entered on the MabThera subcutaneous formulation maintenance therapy once every 8 weeks for 24 months.
anti-rHuPH20 antibodies after treatment with MabThera subcutaneous formulation is not known.
first cycle MabThera intravenous formulation plus 7 cycles of MabThera subcutaneous formulation in combination with up to 8 cycles of CHOP
The recommended dose of MabThera subcutaneous formulation used for adult patients is a subcutaneous injection at a fixed dose of 1400 mg irrespective of the patient's body surface area.
followed by subsequent cycles with MabThera subcutaneous formulation injected at a fixed dose of 1400 mg per cycle.
The objective of the first stage was to establish the rituximab subcutaneous dose that resulted in comparable MabThera subcutaneous formulation serum Ctrough levels compared with MabThera intravenous formulation,
The recommended dose of MabThera subcutaneous formulation used as a maintenance treatment for patients with previously untreated follicular lymphoma who have responded to induction treatment is:
In stage 2, MabThera subcutaneous formulation at a fixed dose of 1400 mg was administered as subcutaneous injection during maintenance treatment,
See Section 5.1. of Herceptin subcutaneous formulation SmPC.
Switching treatment between Herceptin intravenous and Herceptin subcutaneous formulation and vice versa.
Some adverse events/ reactions were reported with a higher frequency for the subcutaneous formulation.
Single doses of up to 960 mg of Herceptin subcutaneous formulation have been administered with no reported untoward effects.
an antihistamine should always be administered before each dose of MabThera subcutaneous formulation.
The safety and efficacy of RoActemra subcutaneous formulation in children from birth to less than 18 years have not been established.