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
88862409 8886240 9 F 2000 20160912 20121105 20160920 EXP US-009507513-1210USA012429 MERCK 0.00 F Y 0.00000 20160920 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
88862409 8886240 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW D 20560 70 MG TABLET /wk
88862409 8886240 2 SS FOSAMAX ALENDRONATE SODIUM 1 D 20560 TABLET
88862409 8886240 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW U 0 70 MG TABLET /wk
88862409 8886240 4 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 35 MG, QW U 0 35 MG TABLET /wk
88862409 8886240 5 C CALCIUM (UNSPECIFIED) CALCIUM 1 Oral UNK, QD U 0 QD
88862409 8886240 6 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK UNK, QD U 0 QD
88862409 8886240 7 C VITAMINS (UNSPECIFIED) VITAMINS 1 Unknown UNK, UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88862409 8886240 1 Osteoporosis
88862409 8886240 2 Osteopenia
88862409 8886240 3 Osteoporosis
88862409 8886240 4 Osteopenia
88862409 8886240 5 Product used for unknown indication
88862409 8886240 6 Product used for unknown indication
88862409 8886240 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
88862409 8886240 OT
88862409 8886240 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
88862409 8886240 Adverse event
88862409 8886240 Anaemia
88862409 8886240 Appendicectomy
88862409 8886240 Back pain
88862409 8886240 Bone disorder
88862409 8886240 Breast tenderness
88862409 8886240 Bronchiectasis
88862409 8886240 Chronic obstructive pulmonary disease
88862409 8886240 Depression
88862409 8886240 Exostosis
88862409 8886240 Extrasystoles
88862409 8886240 Fall
88862409 8886240 Femur fracture
88862409 8886240 Fibromyalgia
88862409 8886240 Glaucoma
88862409 8886240 Hypertension
88862409 8886240 Intervertebral disc degeneration
88862409 8886240 Intramedullary rod insertion
88862409 8886240 Joint effusion
88862409 8886240 Knee operation
88862409 8886240 Meniscal degeneration
88862409 8886240 Osteoarthritis
88862409 8886240 Osteopenia
88862409 8886240 Osteoporosis
88862409 8886240 Osteosclerosis
88862409 8886240 Pain in extremity
88862409 8886240 Pelvic prolapse
88862409 8886240 Product used for unknown indication
88862409 8886240 Prolapse repair
88862409 8886240 Scoliosis
88862409 8886240 Spinal column stenosis
88862409 8886240 Spinal operation
88862409 8886240 Spinal osteoarthritis
88862409 8886240 Synovial cyst
88862409 8886240 Thrombosis
88862409 8886240 Tonsillectomy
88862409 8886240 Vascular calcification
88862409 8886240 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
88862409 8886240 1 2008 0
88862409 8886240 3 200803 200804 0
88862409 8886240 4 2008 2011 0
88862409 8886240 5 1993 0
88862409 8886240 6 2001 0
88862409 8886240 7 1956 0