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
1087956110 10879561 10 F 2005 20160728 20150302 20160802 EXP US-MERCK-1503USA000432 MERCK 0.00 F Y 71.66000 KG 20160802 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
1087956110 10879561 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 10 MG, UNK Y 20560 10 MG TABLET
1087956110 10879561 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK Y 20560 70 MG TABLET
1087956110 10879561 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW Y 20560 70 MG TABLET /wk
1087956110 10879561 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 35 MG, QW Y 20560 35 MG TABLET /wk
1087956110 10879561 5 SS BONIVA IBANDRONATE SODIUM 1 Oral 150 MG, UNK 0 150 MG
1087956110 10879561 6 SS BONIVA IBANDRONATE SODIUM 1 0
1087956110 10879561 7 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNK Y 20560 70 MG TABLET
1087956110 10879561 8 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Y 20560 TABLET
1087956110 10879561 9 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Unknown 70 MG, UNK 0 70 MG
1087956110 10879561 10 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 0
1087956110 10879561 11 C ASCORBIC ACID. ASCORBIC ACID 1 Oral 3 PILLS A DAY OF VITAMIN C W CAL-CITRATE U U 0 200 MG TID
1087956110 10879561 12 C CAL-CITRATE 2 Oral 3 PILLS A DAY OF VITAMIN C W CAL-CITRATE U U 0 200 MG TID
1087956110 10879561 13 C VITAMIN D CHOLECALCIFEROL 1 Oral 2 PILLS A DAY U U 0 200 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1087956110 10879561 1 Osteopenia
1087956110 10879561 2 Osteoporosis postmenopausal
1087956110 10879561 5 Osteopenia
1087956110 10879561 6 Osteoporosis postmenopausal
1087956110 10879561 7 Osteopenia
1087956110 10879561 8 Osteoporosis postmenopausal
1087956110 10879561 9 Osteopenia
1087956110 10879561 10 Osteoporosis postmenopausal
1087956110 10879561 11 Product used for unknown indication
1087956110 10879561 12 Product used for unknown indication
1087956110 10879561 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1087956110 10879561 OT
1087956110 10879561 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1087956110 10879561 Anxiety
1087956110 10879561 Arthralgia
1087956110 10879561 Back pain
1087956110 10879561 Bone loss
1087956110 10879561 Calcium deficiency
1087956110 10879561 Chills
1087956110 10879561 Depression
1087956110 10879561 Femur fracture
1087956110 10879561 Foot fracture
1087956110 10879561 Gait disturbance
1087956110 10879561 Gingival bleeding
1087956110 10879561 Neck pain
1087956110 10879561 Pain in extremity
1087956110 10879561 Periodontal operation
1087956110 10879561 Pollakiuria
1087956110 10879561 Sleep disorder
1087956110 10879561 Treatment noncompliance
1087956110 10879561 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
1087956110 10879561 1 20000712 20001129 0
1087956110 10879561 2 20001221 20060406 0
1087956110 10879561 3 20120717 201302 0
1087956110 10879561 4 20130225 201305 0
1087956110 10879561 5 20060422 20090308 0
1087956110 10879561 7 20120906 201305 0
1087956110 10879561 9 20120906 20130618 0
1087956110 10879561 11 2000 0
1087956110 10879561 12 2000 0
1087956110 10879561 13 2000 0