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
86459917 8645991 7 F 20000904 20160727 20120702 20160801 EXP US-009507513-1206USA04947 MERCK 0.00 F Y 63.95000 KG 20160801 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
86459917 8645991 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral UNK, UNKNOWN 20560 TABLET
86459917 8645991 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 40 MG, 2 Q SUNDAY 20560 40 MG TABLET
86459917 8645991 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
86459917 8645991 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
86459917 8645991 5 C VITAMINS (UNSPECIFIED) VITAMINS 1 Unknown UNK, QD 0 QD
86459917 8645991 6 C SELECTIVE ESTROGEN RECEPTOR MODULATOR (UNSPECIFIED) 2 Unknown UNK, UNKNOWN U 0
86459917 8645991 7 C CORTICOSTEROIDS (UNSPECIFIED) UNSPECIFIED INGREDIENT 1 Unknown UNK, UNKNOWN 0
86459917 8645991 8 C MOTRIN IBUPROFEN 1 Unknown UNK, UNKNOWN U 0
86459917 8645991 9 C MOTRIN IBUPROFEN 1 U 0
86459917 8645991 10 C CORTISONE CORTISONEHYDROCORTISONE 1 Unknown UNK, UNKNOWN U 0
86459917 8645991 11 C RECLAST ZOLEDRONIC ACID 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86459917 8645991 1 Osteoporosis
86459917 8645991 5 Product used for unknown indication
86459917 8645991 6 Product used for unknown indication
86459917 8645991 7 Product used for unknown indication
86459917 8645991 8 Pain in extremity
86459917 8645991 9 Arthralgia
86459917 8645991 10 Arthralgia
86459917 8645991 11 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
86459917 8645991 HO
86459917 8645991 DS
86459917 8645991 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86459917 8645991 Anaemia
86459917 8645991 Arthralgia
86459917 8645991 Arthropathy
86459917 8645991 Asthma
86459917 8645991 Bone lesion
86459917 8645991 Breast cyst
86459917 8645991 Breast cyst excision
86459917 8645991 Bursitis
86459917 8645991 Fall
86459917 8645991 Femur fracture
86459917 8645991 Inappropriate schedule of drug administration
86459917 8645991 Insomnia
86459917 8645991 Internal fixation of fracture
86459917 8645991 Joint crepitation
86459917 8645991 Low turnover osteopathy
86459917 8645991 Medical device pain
86459917 8645991 Musculoskeletal pain
86459917 8645991 Oropharyngeal pain
86459917 8645991 Osteoporosis
86459917 8645991 Seasonal allergy
86459917 8645991 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
86459917 8645991 1 1997 20080529 0
86459917 8645991 2 20000904 0
86459917 8645991 3 20011120 0
86459917 8645991 4 20080602 0
86459917 8645991 5 1990 2012 0
86459917 8645991 6 1990 2008 0
86459917 8645991 7 1994 2007 0