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ג'יוטריף 40 מ"ג GIOTRIF 40 MG (AFATINIB AS DIMALEATE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
פומי : PER OS
צורת מינון:
טבליות מצופות פילם : FILM COATED TABLETS
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Adverse reactions : תופעות לוואי
4.8 Undesirable effects Summary of the safety profile The types of adverse reactions (ADRs) were generally associated with the EGFR inhibitory mode of action of afatinib. The summary of all ADRs is shown in Table 2. The most frequent ADRs were diarrhoea and skin related adverse events (see section 4.4) as well as stomatitis and paronychia (see also Table 3, 4 and 5). Overall, dose reduction (see section 4.2) led to a lower frequency of common adverse reactions. In patients treated with once daily GIOTRIF 40 mg, dose reductions due to ADRs occurred in 57% of the patients in the LUX-Lung 3 trial and in 25% of the patients in the LUX-Lung 8 trial. Discontinuation due to ADRs diarrhoea and rash/acne was 1.3% and 0% in LUX-Lung 3 and 3.8% and 2.0% in LUX-Lung 8, respectively. ILD-like adverse reactions were reported in 0.7% of afatinib treated patients. Bullous, blistering and exfoliative skin conditions have been reported including rare cases suggestive of Stevens-Johnson syndrome and toxic epidermal necrolysis although in these cases there were potential alternative aetiologies (see section 4.4). Tabulated list of adverse reactions Table 2 summarises the frequencies of ADRs from all NSCLC trials and from post-marketing experience with daily GIOTRIF doses of 40 mg or 50 mg as monotherapy. The following terms are used to rank the ADRs by frequency: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000); very rare (<1/10,000). Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. Giotrif Updated Prescribing Information Film coated tablets 20mg, 30mg, 40mg, 50mg December 2019 Table 2: Summary of ADRs per frequency category Body System Very common Common Uncommon Rare Infections and infestations Paronychia1 Cystitis Metabolism and Decreased Dehydration nutrition disorders appetite Hypokalaemia Nervous system disorders Dysgeusia Eye disorders Conjunctivitis Keratitis Dry eye Respiratory, thoracic Interstitial lung and mediastinal Epistaxis Rhinorrhoea disease disorders Gastrointestinal Diarrhoea Pancreatitis disorders Stomatitis2 Dyspepsia Nausea Cheilitis Gastrointestinal Vomiting perforation Hepatobiliary disorders Alanine aminotransferase increased Aspartate aminotransferase increased Skin and subcutaneous Rash3 Stevens-Johnson tissue disorders Palmar-plantar syndrome7 Dermatitis erythrodysaesthesia Toxic epidermal acneiform4 syndrome necrolysis7 Pruritus5 Nail disorders8 Dry skin6 Musculoskeletal and Muscle spasms connective tissue disorders Renal and urinary Renal impairment/ disorders Renal failure General disorders and administration site Pyrexia conditions Investigations Weight decreased 1 Includes Paronychia, Nail infection, Nail bed infection 2 Includes Stomatitis, Aphthous stomatitis, Mucosal inflammation, Mouth ulceration, Oral mucosa erosion, Mucosal erosion, Mucosal ulceration 3 Includes group of rash preferred terms 4 Includes Acne, Acne pustular, Dermatitis acneiform 5 Includes Pruritus, Pruritus generalised 6 Includes Dry skin, Skin chapped 7 Based on post-marketing experience 8 Includes Nail disorder, Onycholysis, Nail toxicity, Onychoclasis, Ingrowing nail, Nail pitting, Onychomadesis, Nail discoloration, Nail dystrophy, Nail ridging, and Onychogryphosis Giotrif Updated Prescribing Information Film coated tablets 20mg, 30mg, 40mg, 50mg December 2019 Description of selected adverse reactions Very common ADRs in GIOTRIF-treated patients occurring in at least 10% of patients in trial LUX-Lung 3 and LUX-Lung 7 are summarised by National Cancer Institute-Common Toxicity Criteria (NCI-CTC) Grade in Tables 3 and 4. Table 3: Very common ADRs in trial LUX-Lung 3 GIOTRIF Pemetrexed/ (40 mg/day) Cisplatin N=229 N=111 NCI-CTC Grade Any 3 4 Any 3 4 Grade Grade MedDRA Preferred Term % % % % % % Infections and infestations Paronychia1 57.6 11.4 0 0 0 0 Metabolism and nutrition disorders Decreased appetite 20.5 3.1 0 53.2 2.7 0 Respiratory, thoracic and mediastinal disorders Epistaxis 13.1 0 0 0.9 0.9 0 Gastrointestinal disorders Diarrhoea 95.2 14.4 0 15.3 0 0 Stomatitis2 69.9 8.3 0.4 13.5 0.9 0 Cheilitis 12.2 0 0 0.9 0 0 Skin and subcutaneous tissue disorders Rash3 70.3 14 0 6.3 0 0 Dermatitis acneiform4 34.9 2.6 0 0 0 0 Dry skin5 29.7 0.4 0 1.8 0 0 Pruritus6 19.2 0.4 0 0.9 0 0 Investigations Weight decreased 10.5 0 0 9.0 0 0 1 Includes Paronychia, Nail infection, Nail bed infection 2 Includes Stomatitis, Aphthous stomatitis, Mucosal inflammation, Mouth ulceration, Oral mucosa erosion, Mucosal erosion, Mucosal ulceration 3 Includes group of rash preferred terms 4 Includes Acne, Acne pustular, Dermatitis acneiform 5 Includes Dry skin, Skin chapped 6 Includes Pruritus, Pruritus generalised Giotrif Updated Prescribing Information Film coated tablets 20mg, 30mg, 40mg, 50mg December 2019 Table 4: Very common ADRs in trial LUX-Lung 7 GIOTRIF Gefitinib (40 mg/day) N=160 N=159 NCI-CTC Grade Any 3 4 Any 3 4 Grade Grade MedDRA Preferred Term % % % % % % Infections and infestations Paronychia1 57.5 1.9 0 17.0 0.6 0 2 Cystitis 11.3 1.3 0 7.5 1.3 0.6 Metabolism and nutrition disorders Decreased appetite 27.5 1.3 0 24.5 1.9 0 3 Hypokalaemia 10.6 2.5 1.3 5.7 1.3 0 Respiratory, thoracic and mediastinal disorders Rhinorrhoea4 19.4 0 0 7.5 0 0 Epistaxis 18.1 0 0 8.8 0 0 Gastrointestinal disorders Diarrhoea 90.6 13.8 0.6 64.2 3.1 0 Stomatitis5 64.4 4.4 0 27.0 0 0 Nausea 25.6 1.3 0 27.7 1.3 0 Vomiting 19.4 0.6 0 13.8 2.5 0 Dyspepsia 10.0 0 0 8.2 0 0 Hepatobiliary disorders Alanine aminotransferase increased 11.3 0 0 27.7 8.8 0.6 Skin and subcutaneous tissue disorders Rash6 80.0 7.5 0 67.9 3.1 0 Dry skin 32.5 0 0 39.6 0 0 Pruritus7 25.6 0 0 25.2 0 0 Dermatitis acneiform8 23.8 1.9 0 32.1 0.6 0 General disorders and administration site conditions Pyrexia 13.8 0 0 6.3 0 0 Investigations Weight decreased 10.0 0.6 0 5.7 0.6 0 1 Includes Paronychia, Nail infection, Nail bed infection 2 Includes Cystitis, Urinary tract infection 3 Includes Hypokalaemia, Blood potassium decreased 4 Includes Rhinorrhoea, Nasal inflammation 5 Includes Stomatitis, Aphthous stomatitis, Mucosal inflammation, Mouth ulceration, Mucosal erosion 6 Includes group of rash preferred terms 7 Includes Pruritus, Pruritus generalised 8 Includes Dermatitis acneiform, Acne Liver function test abnormalities Liver function test abnormalities (including elevated ALT and AST) were observed in patients receiving GIOTRIF 40 mg. These elevations were mainly transient and did not lead to discontinuation. Grade 2 (> 2.5 to 5.0 times upper limit of normal (ULN)) ALT elevations occurred in < 8% of patients treated with this medicinal product. Grade 3 (> 5.0 to 20.0 times ULN) elevations occurred in <4% of patients treated with GIOTRIF (see section 4.4). You can report side effects to the Ministry of Health by following the link ‘Reporting Side Effects of Drug Treatment' on the Ministry of Health home page (www.health.gov.il) which links to an online form for reporting side effects. You can also use this link: https://sideeffects.health.gov.il Giotrif Updated Prescribing Information Film coated tablets 20mg, 30mg, 40mg, 50mg December 2019 Description of selected adverse reactions Very common ADRs in GIOTRIF-treated patients occurring in at least 10% of patients in trial LUX-Lung 8 are summarised by National Cancer Institute-Common Toxicity Criteria (NCI-CTC) Grade in Table 5. Table 5: Very common ADRs in trial LUX-Lung 8* GIOTRIF Erlotinib (40 mg/day) N=395 N=392 NCI-CTC Grade Any 3 4 Any 3 4 Grade Grade MedDRA Preferred Term % % % % % % Infections and infestations Paronychia1 11.0 0.5 0 5.1 0.3 0 Metabolism and nutrition disorders Decreased appetite 24.7 3.1 0 26.1 2.0 0 Gastrointestinal disorders Diarrhoea 74.7 9.9 0.8 41.3 3.0 0.3 Stomatitis2 30.1 4.1 0 10.6 0.5 0 Nausea 20.7 1.5 0 16.2 1.0 0.3 Skin and subcutaneous tissue disorders Rash3 60.7 5.4 0 56.7 8.1 0 Dermatitis acneiform4 14.0 1.3 0 18.0 2.5 0 * Reporting the frequency of patients with all causality AEs 1 Includes Paronychia, Nail infection, Nail bed infection 2 Includes Stomatitis, Aphthous stomatitis, Mucosal inflammation, Mouth ulceration, Oral mucosa erosion, Mucosal erosion, Mucosal ulceration 3 Includes group of rash preferred terms 4 Includes Acne, Acne pustular, Dermatitis acneiform Liver function test abnormalities Liver function test abnormalities (including elevated ALT and AST) were observed in patients receiving GIOTRIF 40 mg. These elevations were mainly transient and did not lead to discontinuation. Grade 2 ALT elevations occurred in 1% and Grade 3 elevations occurred in 0.8% of patients treated with GIOTRIF (see section 4.4).
פרטי מסגרת הכללה בסל
1. התרופה תינתן לטיפול בסרטן ריאה מתקדם מקומי או גרורתי מסוג non small cell: א. כקו טיפול ראשון לחולים המבטאים מוטציה ב-EGFR; ב. לאחר כשל בטיפול קודם בתרופה אחרת המיועדת להתוויה זו, לקו טיפול שני או שלישי, המבטאים מוטציה ב-EGFR. 2. קיבל החולה טיפול באחת מהתרופות Afatinib או Erlotinib או Gefitinib, לא יקבל טיפול בתרופה האחרת, למחלה זו. 3. מתן התרופה האמורה ייעשה לפי מרשם של מומחה באונקולוגיה.
מסגרת הכללה בסל
התוויות הכלולות במסגרת הסל
התוויה | תאריך הכללה | תחום קליני | Class Effect | מצב מחלה |
---|---|---|---|---|
התרופה תינתן לטיפול בסרטן ריאה מתקדם מקומי או גרורתי מסוג non small cell | 12/01/2014 |
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
12/01/2014
הגבלות
תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת
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ג'יוטריף 40 מ"ג