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
97336993 9733699 3 F 2009 20160808 20131205 20160812 EXP US-009507513-1312USA001819 MERCK 0.00 F Y 0.00000 20160812 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
97336993 9733699 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
97336993 9733699 2 SS FOSAMAX ALENDRONATE SODIUM 1 U 20560 TABLET
97336993 9733699 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN U 0 70 MG
97336993 9733699 4 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 U 0
97336993 9733699 5 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN U 0 70 MG
97336993 9733699 6 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN U 0 70 MG
97336993 9733699 7 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN U 0 70 MG
97336993 9733699 8 C VITAMINS (UNSPECIFIED) VITAMINS 1 Oral 1 TABLET, UNKNOWN U 0
97336993 9733699 9 C CALCIUM (UNSPECIFIED) CALCIUM 1 Oral 1 TABLET, UNKNOWN U U 0
97336993 9733699 10 C ASCORBIC ACID. ASCORBIC ACID 1 Oral 1 TAB, UNKNOWN U U 0
97336993 9733699 11 C chondroitin sulfate sodium (+) glucosamine sulfate 2 Oral 1 TABLET, UNKNOWN U 0
97336993 9733699 12 C ASPIRIN. ASPIRIN 1 Oral 1 TABLET, UNKNOWN U 0
97336993 9733699 13 C MELATONIN MELATONIN 1 Oral 1 TABLET, UNKNOWN U 0
97336993 9733699 14 C ALEVE NAPROXEN SODIUM 1 Oral UNK UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97336993 9733699 1 Osteoporosis prophylaxis
97336993 9733699 2 Osteoporosis
97336993 9733699 3 Osteoporosis prophylaxis
97336993 9733699 4 Osteoporosis
97336993 9733699 5 Osteoporosis
97336993 9733699 6 Osteoporosis
97336993 9733699 7 Osteoporosis
97336993 9733699 8 Product used for unknown indication
97336993 9733699 9 Product used for unknown indication
97336993 9733699 10 Product used for unknown indication
97336993 9733699 11 Product used for unknown indication
97336993 9733699 12 Product used for unknown indication
97336993 9733699 13 Product used for unknown indication
97336993 9733699 14 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
97336993 9733699 HO
97336993 9733699 OT
97336993 9733699 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
97336993 9733699 Arthritis
97336993 9733699 Cataract operation
97336993 9733699 Cholecystectomy
97336993 9733699 Dementia
97336993 9733699 Depression
97336993 9733699 Essential hypertension
97336993 9733699 Fall
97336993 9733699 Femur fracture
97336993 9733699 Haemarthrosis
97336993 9733699 Hypertension
97336993 9733699 Infection
97336993 9733699 Knee arthroplasty
97336993 9733699 Low turnover osteopathy
97336993 9733699 Muscle strain
97336993 9733699 Osteoporosis
97336993 9733699 Pain in extremity
97336993 9733699 Peripheral swelling

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
97336993 9733699 1 20070321 200803 0
97336993 9733699 3 20080310 201110 0
97336993 9733699 5 201009 201011 0
97336993 9733699 6 201011 201102 0
97336993 9733699 7 201103 201201 0
97336993 9733699 8 2007 0
97336993 9733699 9 2007 0
97336993 9733699 10 2007 0
97336993 9733699 11 2007 0
97336993 9733699 12 2007 0
97336993 9733699 13 2007 0
97336993 9733699 14 2000 0