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
117524035 11752403 5 F 20151018 20160629 20151118 20160706 EXP JP-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2015-BI-64381NB BOEHRINGER INGELHEIM 69.96 YR F Y 44.00000 KG 20160706 MD JP JP

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
117524035 11752403 1 PS GILOTRIF AFATINIB 1 Oral 40 MG 201292 40 MG FILM COATED TABLET QD
117524035 11752403 2 SS LOPERAMIDE LOPERAMIDE 1 Oral 2 MG 0 2 MG QD
117524035 11752403 3 C DENOTAS CALCIUM CARBONATECHOLECALCIFEROLMAGNESIUM CARBONATE 1 Oral 2 ANZ 0 TABLET QD
117524035 11752403 4 C RANMARK DENOSUMAB 1 Subcutaneous 120 MG 0 120 MG INJECTION QD
117524035 11752403 5 C BROTIZOLAM BROTIZOLAM 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117524035 11752403 1 Lung adenocarcinoma
117524035 11752403 2 Prophylaxis against diarrhoea
117524035 11752403 3 Prophylaxis
117524035 11752403 4 Metastases to bone
117524035 11752403 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117524035 11752403 LT
117524035 11752403 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117524035 11752403 Decreased appetite
117524035 11752403 Diarrhoea
117524035 11752403 Rash
117524035 11752403 Toxic epidermal necrolysis
117524035 11752403 Vomiting

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
117524035 11752403 1 20151017 20151109 0
117524035 11752403 2 20151012 0
117524035 11752403 3 20140729 0
117524035 11752403 4 20140729 0