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
125636321 12563632 1 I 20160708 20160708 20160715 20160715 EXP PHHY2016BR096934 NOVARTIS 53.55 YR M Y 0.00000 20160716 OT BR 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
125636321 12563632 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, QD SC680/ 704710 21817 1 DF SOLUTION FOR INJECTION QD
125636321 12563632 2 C CRESTOR ROSUVASTATIN CALCIUM 1 Unknown U 0
125636321 12563632 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown U 0
125636321 12563632 4 C FINASTERIDE. FINASTERIDE 1 Unknown U 0
125636321 12563632 5 C ARTROLIVE CHONDROITIN SULFATE (BOVINE)GLUCOSAMINE SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125636321 12563632 1 Osteoporosis
125636321 12563632 2 Product used for unknown indication
125636321 12563632 3 Product used for unknown indication
125636321 12563632 4 Product used for unknown indication
125636321 12563632 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125636321 12563632 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125636321 12563632 Anxiety
125636321 12563632 Pain
125636321 12563632 Pyrexia
125636321 12563632 Syncope
125636321 12563632 Vagus nerve disorder

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
125636321 12563632 1 20160707 20160707 0