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
86840247 8684024 7 F 2005 20160803 20120726 20160808 EXP US-009507513-1207USA005636 MERCK 0.00 F Y 68.48000 KG 20160808 MD 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
86840247 8684024 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN 20560 70 MG TABLET
86840247 8684024 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 35 MG, UNK 20560 35 MG TABLET
86840247 8684024 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral UNK UNK, UNKNOWN 20560 TABLET
86840247 8684024 4 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral 70 MG, UNK 0 70 MG TABLET
86840247 8684024 5 C CENTRUM SILVER MINERALSVITAMINS 1 Unknown UNK, QD 0 QD
86840247 8684024 6 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN 0 70 MG TABLET
86840247 8684024 7 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 0 TABLET
86840247 8684024 8 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN 0 70 MG TABLET
86840247 8684024 9 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 0 TABLET
86840247 8684024 10 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNKNOWN 0 70 MG TABLET
86840247 8684024 11 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86840247 8684024 1 Osteoporosis prophylaxis
86840247 8684024 2 Osteoporosis
86840247 8684024 4 Osteoporosis
86840247 8684024 6 Osteoporosis
86840247 8684024 7 Osteoporosis prophylaxis
86840247 8684024 8 Osteoporosis
86840247 8684024 9 Osteoporosis prophylaxis
86840247 8684024 10 Osteoporosis
86840247 8684024 11 Osteoporosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
86840247 8684024 HO
86840247 8684024 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86840247 8684024 Ankle fracture
86840247 8684024 Arthritis
86840247 8684024 Asthma
86840247 8684024 Bone infarction
86840247 8684024 Cardiac murmur
86840247 8684024 Chronic obstructive pulmonary disease
86840247 8684024 Contusion
86840247 8684024 Cough
86840247 8684024 Cyst
86840247 8684024 Dyslipidaemia
86840247 8684024 Femur fracture
86840247 8684024 Fracture reduction
86840247 8684024 Gastrooesophageal reflux disease
86840247 8684024 Hand fracture
86840247 8684024 Hypertension
86840247 8684024 Hysterectomy
86840247 8684024 Infection
86840247 8684024 Intramedullary rod insertion
86840247 8684024 Joint injury
86840247 8684024 Kyphosis
86840247 8684024 Loss of libido
86840247 8684024 Macular degeneration
86840247 8684024 Oedema peripheral
86840247 8684024 Pulmonary embolism
86840247 8684024 Restless legs syndrome
86840247 8684024 Vitamin D decreased
86840247 8684024 Xerosis

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
86840247 8684024 1 200512 200703 0
86840247 8684024 2 2007 0
86840247 8684024 3 2002 2012 0
86840247 8684024 4 200512 200601 0
86840247 8684024 5 1975 0
86840247 8684024 6 200802 200906 0
86840247 8684024 8 201110 201206 0
86840247 8684024 10 201108 201109 0