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
117983692 11798369 2 F 20151013 20160627 20151203 20160701 EXP PHHY2015VE125361 NOVARTIS 52.76 YR F Y 0.00000 20160701 CN COUNTRY NOT SPECIFIED VE

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
117983692 11798369 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD Y 22334 10 MG QD
117983692 11798369 2 C COAPROVEL HYDROCHLOROTHIAZIDEIRBESARTAN 1 Unknown 150 MG, UNK U 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117983692 11798369 1 Breast cancer
117983692 11798369 2 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
117983692 11798369 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117983692 11798369 Asthenia
117983692 11798369 Bone pain
117983692 11798369 Drug ineffective
117983692 11798369 Gait disturbance
117983692 11798369 Haemorrhoids
117983692 11798369 Malaise
117983692 11798369 Mouth ulceration
117983692 11798369 Nervousness
117983692 11798369 Pain

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
117983692 11798369 1 20151011 0