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
99299616 9929961 6 F 20140203 20160919 20140227 20160923 EXP PHHO2014FR001984 SANDOZ 74.00 YR M Y 71.80000 KG 20160923 MD FR FR

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
99299616 9929961 1 SS BKM120 BUPARLISIB HYDROCHLORIDE 1 Oral 100 MG, QD 500 MG Y 0 100 MG CAPSULE QD
99299616 9929961 2 PS CANDESARTAN CILEXETIL. CANDESARTAN CILEXETIL 1 Unknown 16 MG, PER DAY Y 78702 16 MG QD
99299616 9929961 3 C PARACETAMOL CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 2 G, PER DAY 0 2 G QD
99299616 9929961 4 C PREGABALIN. PREGABALIN 1 375 MG, PER DAY 0 375 MG QD
99299616 9929961 5 C LEVOTHYROXIN LEVOTHYROXINE 1 200 UG, PER DAY 0 200 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99299616 9929961 1 Head and neck cancer metastatic
99299616 9929961 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
99299616 9929961 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
99299616 9929961 Dehydration
99299616 9929961 Hypotension

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
99299616 9929961 1 20140129 20140202 0
99299616 9929961 2 2009 20140204 0
99299616 9929961 3 201312 0
99299616 9929961 4 201312 0
99299616 9929961 5 2006 0