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
90098243 9009824 3 F 200006 20160805 20130110 20160815 EXP US-009507513-1301USA002415 MERCK 0.00 F Y 0.00000 20160815 LW US US

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
90098243 9009824 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
90098243 9009824 2 SS BONIVA IBANDRONATE SODIUM 1 Oral 150 MG, UNK U 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90098243 9009824 1 Osteoporosis
90098243 9009824 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
90098243 9009824 OT
90098243 9009824 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90098243 9009824 Accident
90098243 9009824 Aortic arteriosclerosis
90098243 9009824 Balance disorder
90098243 9009824 Blood cholesterol increased
90098243 9009824 Cerebellar infarction
90098243 9009824 Cerebral infarction
90098243 9009824 Cognitive disorder
90098243 9009824 Fall
90098243 9009824 Femur fracture
90098243 9009824 Fracture
90098243 9009824 Haemorrhoids
90098243 9009824 Headache
90098243 9009824 Hyperlipidaemia
90098243 9009824 Hypertension
90098243 9009824 Memory impairment
90098243 9009824 Orthostatic hypotension
90098243 9009824 Tooth 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
90098243 9009824 1 2000 200705 0
90098243 9009824 2 200602 201201 0