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
124878113 12487811 3 F 20160811 20160622 20160816 EXP PHHY2016CA083306 NOVARTIS 0.00 F Y 0.00000 20160816 CN COUNTRY NOT SPECIFIED CA

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
124878113 12487811 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION
124878113 12487811 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG/DL, UNK 21817 SOLUTION FOR INJECTION
124878113 12487811 3 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG/DL, UNK 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124878113 12487811 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
124878113 12487811 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124878113 12487811 Arthralgia
124878113 12487811 Drug ineffective
124878113 12487811 Pneumonia

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
124878113 12487811 1 20130703 0
124878113 12487811 2 20140702 0
124878113 12487811 3 20150703 0