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
87697144 8769714 4 F 200509 20160816 20120905 20160822 EXP US-009507513-1208USA010563 MERCK 0.00 F Y 0.00000 20160822 PH 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
87697144 8769714 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QD 32620 MG 20560 70 MG TABLET QD
87697144 8769714 2 SS BONIVA IBANDRONATE SODIUM 1 Oral 150 MG, UNK U 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87697144 8769714 1 Osteopenia
87697144 8769714 2 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
87697144 8769714 OT
87697144 8769714 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
87697144 8769714 Anxiety
87697144 8769714 Depression
87697144 8769714 Femur fracture
87697144 8769714 Hypothyroidism
87697144 8769714 Impaired healing
87697144 8769714 Inappropriate schedule of drug administration
87697144 8769714 Incisional drainage
87697144 8769714 Osteonecrosis
87697144 8769714 Post procedural haematoma
87697144 8769714 Spinal operation
87697144 8769714 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
87697144 8769714 1 20050929 20070107 0
87697144 8769714 2 200707 201203 0