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
125545271 12554527 1 I 20160222 20160713 20160713 PER US-ROCHE-1716536 ROCHE 0.00 F Y 0.00000 20160713 CN 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
125545271 12554527 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown U 21455 TABLET
125545271 12554527 2 SS RECLAST ZOLEDRONIC ACID 1 Unknown U 0
125545271 12554527 3 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown U 0
125545271 12554527 4 C FORTEO TERIPARATIDE 1 0
125545271 12554527 5 C ACTONEL RISEDRONATE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125545271 12554527 1 Osteoporosis
125545271 12554527 2 Product used for unknown indication
125545271 12554527 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125545271 12554527 Coeliac disease
125545271 12554527 Dyspepsia
125545271 12554527 Hypersensitivity
125545271 12554527 Osteoporosis
125545271 12554527 Photosensitivity reaction
125545271 12554527 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found