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
126167106 12616710 6 F 20160726 20160912 20160802 20160915 EXP PHHY2016BR105756 NOVARTIS 70.61 YR F Y 69.00000 KG 20160915 CN COUNTRY NOT SPECIFIED BR

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
126167106 12616710 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG/100ML Q12MO SC045 21817 5 MG SOLUTION FOR INJECTION
126167106 12616710 2 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown U 0
126167106 12616710 3 C LYRICA PREGABALIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126167106 12616710 1 Osteoporosis
126167106 12616710 2 Product used for unknown indication
126167106 12616710 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126167106 12616710 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126167106 12616710 Anxiety
126167106 12616710 Drug ineffective
126167106 12616710 Headache
126167106 12616710 Pain
126167106 12616710 Temporal arteritis

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
126167106 12616710 1 20160726 20160726 0