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
97068924 9706892 4 F 2009 20160923 20131125 20160930 EXP US-009507513-1311USA007339 MERCK 0.00 F Y 0.00000 20160930 MD 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
97068924 9706892 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 75 MG QW D 20560 TABLET
97068924 9706892 2 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral 75 MG QW 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97068924 9706892 1 Osteoporosis
97068924 9706892 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
97068924 9706892 DS
97068924 9706892 HO
97068924 9706892 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97068924 9706892 Back injury
97068924 9706892 Blood cholesterol increased
97068924 9706892 Blood pressure increased
97068924 9706892 Calcium deficiency
97068924 9706892 Cataract
97068924 9706892 Fall
97068924 9706892 Femur fracture
97068924 9706892 Fracture
97068924 9706892 Fungal infection
97068924 9706892 Gastrooesophageal reflux disease
97068924 9706892 Incorrect dose administered
97068924 9706892 Joint injury
97068924 9706892 Limb injury
97068924 9706892 Macular degeneration
97068924 9706892 Osteoporosis
97068924 9706892 Skin abrasion
97068924 9706892 Spinal flattening
97068924 9706892 Vitamin D deficiency

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
97068924 9706892 1 2000 20061209 0
97068924 9706892 2 20061209 2010 0