The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126068411 12606841 1 I 20160718 20160729 20160729 EXP BE-TEVA-680776ISR TEVA SZTURZ P, SPECENIER P, VAN LAER C, VAN DEN WEYNGAERT D, CORTHOUTS B, CARP L, ET AL. LONG-TERM REMISSION OF LOCALLY RECURRENT OROPHARYNGEAL CANCER AFTER DOCETAXEL-BASED CHEMOTHERAPY PLUS CETUXIMAB. EUR-ARCH-OTORHINOLARYNGOL 2016;273(6):1629-1636. 0.00 A M Y 0.00000 20160729 OT BE BE

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126068411 12606841 1 PS CISPLATIN. CISPLATIN 1 Unknown 75 MG/M2 DAILY; 75 MG/M2 ON DAY 1 Y 74656 Q3W
126068411 12606841 2 SS CISPLATIN. CISPLATIN 1 Unknown 100 MG/M2 DAILY; 100 MG/M2 ON DAY 1 Y 74656 Q3W
126068411 12606841 3 SS FLUOROURACIL. FLUOROURACIL 1 Unknown 750 MG/M2 DAILY; 750 MG/M2 ON DAYS 1-5 Y 40333 Q3W
126068411 12606841 4 SS FLUOROURACIL. FLUOROURACIL 1 Unknown 1000 MG/M2 DAILY; 1000 MG/M2 ON DAYS 1-4 Y 40333 Q3W
126068411 12606841 5 SS DOCETAXEL. DOCETAXEL 1 Unknown 75 MG/M2 DAILY; 75 MG/M2 ON DAY 1 Y 0 Q3W
126068411 12606841 6 SS cetuximab CETUXIMAB 1 Unknown 250 MG/M2 DAILY; 250 MG/M2 ON DAYS 1,8 AND 15 Y 0 Q3W
126068411 12606841 7 SS cetuximab CETUXIMAB 1 Unknown 400 MG/M2 DAILY; 400 MG/M2 ON DAY 1 (LOADING DOSE) Y 0
126068411 12606841 8 SS cetuximab CETUXIMAB 1 Unknown 250 MG/M2 DAILY; 250 MG/M2 WEEKLY (MAINTENANCE DOSE) Y 0 /wk
126068411 12606841 9 SS cetuximab CETUXIMAB 1 Unknown 250 MG/M2 DAILY; 250 MG/M2 WEEKLY (MAINTENANCE DOSE) Y 0 /wk
126068411 12606841 10 SS cetuximab CETUXIMAB 1 Unknown 400 MG/M2 DAILY; 400 MG/M2 WEEKLY (INITIAL DOSE) Y 0
126068411 12606841 11 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 16 MILLIGRAM DAILY; 0 8 MG BID
126068411 12606841 12 C CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 1000 MILLIGRAM DAILY; 500MG EVERY 12 HOURS ON DAYS 5-15 U 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126068411 12606841 1 Oropharyngeal cancer recurrent
126068411 12606841 3 Oropharyngeal cancer recurrent
126068411 12606841 5 Oropharyngeal cancer recurrent
126068411 12606841 6 Oropharyngeal cancer recurrent
126068411 12606841 12 Antibiotic prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126068411 12606841 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126068411 12606841 Alopecia
126068411 12606841 Constipation
126068411 12606841 Deafness
126068411 12606841 Decreased appetite
126068411 12606841 Diarrhoea
126068411 12606841 Dizziness
126068411 12606841 Fatigue
126068411 12606841 Febrile neutropenia
126068411 12606841 Hypotension
126068411 12606841 Infection
126068411 12606841 Nail disorder
126068411 12606841 Nausea
126068411 12606841 Neutropenia
126068411 12606841 Performance status decreased
126068411 12606841 Peripheral sensory neuropathy
126068411 12606841 Punctate keratitis
126068411 12606841 Rash
126068411 12606841 Stomatitis
126068411 12606841 Visual acuity reduced
126068411 12606841 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126068411 12606841 1 20060614 20060916 0
126068411 12606841 2 20050509 20050906 0
126068411 12606841 3 20060614 20060916 0
126068411 12606841 4 20050509 20050906 0
126068411 12606841 5 20060614 20060916 0
126068411 12606841 6 20060614 20060916 0
126068411 12606841 7 20060614 0
126068411 12606841 8 20050913 20060503 0
126068411 12606841 9 20050509 20050906 0
126068411 12606841 10 20050509 0