La survenue transitoire, quelques heures après l'administration du traitement, de frissons, fièvre ou syndromes pseudo-grippaux, a été rapportée (chez respectivement 3%, 2% et 1% des patients).Les principaux effets indésirables au site d'injection ont été une douleur et un érythème, rapportés respectivement chez 28% et 17% des patients. It is used to treat advanced prostate cancer that is dependent on hormones for growth. You may report side effects to FDA at 1-800-FDA-1088.Tell your healthcare provider if you have any side effects that bother you or that does not go away. The majority of the adverse reactions were Grade 1 or 2, with Grade 3/4 adverse reaction incidences of 1% or less.Adverse reactions reported in ≥ 5% of patients treated with FIRMAGON (subcutaneous) 240 mg starting dose and then 80 mg maintenance dose once every 28 days or who were treated with 7.5 mg of leuprolide (intramuscular) every 28 days are shown in Table 2.The following adverse reactions occurred in 1 to < 5% of patients treated with FIRMAGON:The following adverse reactions, not already listed, occurred in ≥ 1% of patients treated in any study with FIRMAGON:The most frequently reported adverse reactions at the injection sites were pain (28%), erythema (17%), swelling (6%), induration (4%) and nodule (3%). When injected, Firmagon forms a gel under the skin that releases the active substance slowly over a few weeks.The effects of Firmagon were first tested in experimental models before being studied in humans.Two doses of Firmagon have been compared with leuprorelin in one main study involving 610 men with prostate cancer at all stages of the disease. FIRMAGON is an injectable gonadotropin-releasing hormone (GnRH) receptor antagonist approved in 2009 by the U.S. Food and Drug Administration (FDA) for the treatment of … The most common adverse reactions reported in ≥10% of the patients were injection site reactions (e.g., pain, erythema, swelling, induration or inflammation), pyrexia, hot flush, weight loss or gain, fatigue, increases in serum levels of hepatic transaminases and GGT. You may report side effects to FDA at 1-800-FDA-1088.FERRING, the FERRING PHARMACEUTICALS logo, and other Ferring product trade names are trademarks of Ferring B.V. save where indicated otherwise.Tell your healthcare provider if you have any side effects that bother you or that does not go away. Doctors should monitor the effectiveness of Firmagon treatment by looking at blood levels of testosterone and prostate-specific antigen (PSA). Firmagon must not be injected into a vein or a muscle. Une marque spécifique de ce médicament n'est peut-être pas offerte sous toutes les for… With Firmagon my T-level dropped almost immediately to a new low (and the PSA did the same). La part qui revient au cancer de la prostate ou à la suppression androgénique pour expliquer cette diminution n'est pas clairement définie. That was very successful, so I am a bit hesitant to switch back to an agonist. Ce médicament est disponible sous divers noms de marque ou sous différentes présentations. How degarelix works. Les événements rapportés ont été le plus souvent transitoires, d'intensité faible à modérée et n'ont conduit que très rarement à l'arrêt du traitement (<1%). You may report side effects to FDA at 1-800-FDA-1088.Tell your healthcare provider if you have any side effects that bother you or that does not go away. et des produits de santé (ANSM). amiodarone, sotalol, dofétilide, ibutilide), méthadone, cisapride, moxifloxacine, antipsychotiques, etc., doit être évaluée avec précaution (voir rubrique Mises en garde et précautions d'emploi). Chez les patients ayant des valeurs normales avant le traitement, des valeurs nettement anormales de kaliémie (≥ 5,8 mmol/l), de créatininémie (≥177 µmol/l) et d'urée sanguine (≥10,7 mmol/l) ont été observées respectivement chez 6%, 2% et 15 % des patients traités par dégarélix et chez 3%, 2% et 14% des patients traités par leuproréline.Les modifications observées à l'ECG au cours d'une année de traitement dans l'étude pivot de phase III (N = 409) ont été similaires avec les 2 produits : dégarélix et un agoniste à la GnRH (leuproréline) utilisé comme comparateur. Anyhow, next step is to have another test of my T-level one week after the injection of the Firmagon to get a better idea of the dynamics of my T-level between two shots. Toutes les infos sur ce médicament There is no indication that the efficacy or safety of FIRMAGON treatment is affected by antibody formation.The following adverse reactions have been identified during post-approval use of FIRMAGON. You may report side effects to FDA at 1-800-FDA-1088.Tell your healthcare provider if you have any side effects that bother you or that does not go away. You may report side effects to FDA at 1-800-FDA-1088.I like the regularity of the monthly shot and the chance it gives me to build a relationship with my treatment team.
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