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
108642673 10864267 3 F 20060110 20160808 20150224 20160812 EXP US-009507513-1502USA009211 MERCK 0.00 F Y 0.00000 20160812 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
108642673 10864267 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
108642673 10864267 2 SS FOSAMAX ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 3 SS FOSAMAX ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 4 SS FOSAMAX ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 5 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral 70 MG, QW 0 70 MG TABLET /wk
108642673 10864267 6 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
108642673 10864267 7 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 8 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 9 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 20560 TABLET
108642673 10864267 10 C CALCIUM (UNSPECIFIED) CALCIUM 1 Oral 1200 MG, QD 0 1200 MG QD
108642673 10864267 11 C VITAMIN D CHOLECALCIFEROL 1 Unknown UNK, QD 0 QD
108642673 10864267 12 C LODINE ETODOLAC 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108642673 10864267 1 Osteoporosis prophylaxis
108642673 10864267 2 Osteoporosis
108642673 10864267 3 Osteopenia
108642673 10864267 4 Prophylaxis
108642673 10864267 5 Osteoporosis
108642673 10864267 6 Osteoporosis prophylaxis
108642673 10864267 7 Osteoporosis
108642673 10864267 8 Osteopenia
108642673 10864267 9 Prophylaxis
108642673 10864267 12 Arthropathy

Outcome of event

Event ID CASEID OUTC COD
108642673 10864267 OT
108642673 10864267 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108642673 10864267 Ankle fracture
108642673 10864267 Blood cholesterol increased
108642673 10864267 Carotid artery stenosis
108642673 10864267 Drug hypersensitivity
108642673 10864267 Fall
108642673 10864267 Femur fracture
108642673 10864267 Foot fracture
108642673 10864267 Hyperlipidaemia
108642673 10864267 Hypertension
108642673 10864267 Intervertebral disc degeneration
108642673 10864267 Knee arthroplasty
108642673 10864267 Low turnover osteopathy
108642673 10864267 Lung disorder
108642673 10864267 Migraine
108642673 10864267 Pain in extremity
108642673 10864267 Stress fracture
108642673 10864267 Vitamin D deficiency
108642673 10864267 Vomiting

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
108642673 10864267 1 200601 200705 0
108642673 10864267 5 200705 200901 0
108642673 10864267 6 200901 201303 0
108642673 10864267 10 1996 0
108642673 10864267 11 1996 0
108642673 10864267 12 2004 2014 0