Примери за използване на Tobi podhaler на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
How much TOBI Podhaler to take.
Other medicines and TOBI Podhaler.
TOBI Podhaler capsules must not be swallowed.
Do not swallow TOBI Podhaler capsules.
TOBI Podhaler 28 mg inhalation powder, hard capsules.
How long to take TOBI Podhaler.
TOBI Podhaler is a powder for inhalation that is filled into capsules.
What benefit has Tobi Podhaler shown during the studies?
No interaction studies have been performed with TOBI Podhaler.
Continue taking TOBI Podhaler as your doctor tells you.
CHMP also noted the differences in terms of inhalation time between Tobramycin VVB and Tobi Podhaler.
Always keep the TOBI Podhaler capsules and device in a dry place.
A risk management plan has been developed to ensure that Tobi Podhaler is used as safely as possible.
TOBI Podhaler 28 mg inhalation powder, hard capsules Tobramycin.
The maximum tolerated daily dose of TOBI Podhaler has not been established.
TOBI Podhaler contains a medicine called tobramycin which is an antibiotic.
For more information on how to use Tobi Podhaler, see the instructions in the package leaflet.
Tobi Podhaler is inhaled using a hand-held device called Podhaler. .
For more information about treatment with Tobi Podhaler, read the package leaflet(also part of the EPAR) or contact your doctor or pharmacist.
Tobi Podhaler is a medicine that contains the active substance tobramycin.
After four weeks of treatment,the patients taking Tobi Podhaler had an improvement in FEV1 of 13.2%, while patients taking placebo had a reduction in FEV1 of around 0.6%.
Tobi Podhaler is intended to increase the convenience of taking tobramycin for patients.
The summary of the opinion of the Committee for Orphan Medicinal Products for Tobi Podhaler can be found on the Agency's website ema. europa. eu/Find medicine/Human medicines/Rare disease designation.
Tobi Podhaler was more effective than placebo in treating P. aeruginosa infection in patients with cystic fibrosis.
Demonstration of clinical superiority is required because Tobi Podhaler is an orphan medicine and was granted market exclusivity in the EU at the time of its market authorisation in July 2011.
Tobi Podhaler was studied in two main trials in patients who had cystic fibrosis with P. aeruginosa lung infection.
The first trial, which involved 102 patients aged 6 to 21 years,compared Tobi Podhaler with placebo(a dummy treatment), while the second, involving 553 mostly adult patients, compared it with Tobi. .
Tobi Podhaler must not be used in people who are hypersensitive(allergic) to tobramycin, any aminoglycoside or any of the other ingredients.
Based on this plan, safety information has been included in the summary of product characteristics and the package leaflet for Tobi Podhaler, including the appropriate precautions to be followed by healthcare professionals and patients.
The effect of Tobi Podhaler was similar to that of Tobi after three cycles of treatment.