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
127763852 12776385 2 F 20160910 20160923 20160923 20160930 EXP PHHY2016FR130069 NOVARTIS 67.00 YR F Y 0.00000 20160930 CN 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
127763852 12776385 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK D 21817 5 MG SOLUTION FOR INJECTION
127763852 12776385 2 C PREVISCAN FLUINDIONE 1 Oral 0.5 DF, QD Y 0 .5 DF QD
127763852 12776385 3 C PREVISCAN FLUINDIONE 1 Oral 0.25 DF, QD Y 0 .25 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127763852 12776385 1 Osteoporosis
127763852 12776385 2 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127763852 12776385 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127763852 12776385 Diabetes mellitus
127763852 12776385 Fatigue
127763852 12776385 Haemophilia
127763852 12776385 Influenza like illness
127763852 12776385 International normalised ratio increased
127763852 12776385 Nausea
127763852 12776385 Pyrexia
127763852 12776385 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
127763852 12776385 1 20160909 0
127763852 12776385 2 20160910 0
127763852 12776385 3 20160910 0