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
89088716 8908871 6 F 200309 20160902 20121114 20160913 EXP US-009507513-1211USA002775 MERCK 0.00 F Y 60.32000 KG 20160913 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
89088716 8908871 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
89088716 8908871 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
89088716 8908871 3 SS FOSAMAX ALENDRONATE SODIUM 1 35 MG, QW 20560 35 MG TABLET /wk
89088716 8908871 4 C PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 Unknown 0.625 MG, QD U 0 .626 MG QD
89088716 8908871 5 C VITAMIN A VITAMIN A 1 Unknown UNK UNK, UNKNOWN U 0
89088716 8908871 6 C VITAMIN D CHOLECALCIFEROL 1 Unknown 600-800 IU, UNK U 0 800 IU
89088716 8908871 7 C VITAMIN E .ALPHA.-TOCOPHEROL 1 Unknown UNK, UNKNOWN U 0
89088716 8908871 8 C CALCIUM (UNSPECIFIED) CALCIUM 1 Unknown 1500 DF, UNKNOWN U 0 1500 DF
89088716 8908871 9 C CALCIUM (UNSPECIFIED) CALCIUM 1 1800 MG, QD U 0 1800 MG QD
89088716 8908871 10 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Unknown 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89088716 8908871 1 Osteoporosis
89088716 8908871 4 Hormone therapy
89088716 8908871 5 Product used for unknown indication
89088716 8908871 6 Product used for unknown indication
89088716 8908871 7 Product used for unknown indication
89088716 8908871 8 Product used for unknown indication
89088716 8908871 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
89088716 8908871 OT
89088716 8908871 HO
89088716 8908871 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
89088716 8908871 Acetabulum fracture
89088716 8908871 Ankle fracture
89088716 8908871 Barrett's oesophagus
89088716 8908871 Blood cholesterol increased
89088716 8908871 Blood urea increased
89088716 8908871 Bone disorder
89088716 8908871 Bone metabolism disorder
89088716 8908871 Calcium deficiency
89088716 8908871 Depression
89088716 8908871 Drug ineffective
89088716 8908871 Femur fracture
89088716 8908871 Fractured ischium
89088716 8908871 Gastrooesophageal reflux disease
89088716 8908871 Herpes zoster
89088716 8908871 Hip fracture
89088716 8908871 Hyperlipidaemia
89088716 8908871 Impaired healing
89088716 8908871 Low turnover osteopathy
89088716 8908871 Lower limb fracture
89088716 8908871 Mobility decreased
89088716 8908871 Nasal septum deviation
89088716 8908871 Nausea
89088716 8908871 Osteoarthritis
89088716 8908871 Osteoporosis
89088716 8908871 Periodontal disease
89088716 8908871 Periodontal operation
89088716 8908871 Pubis fracture
89088716 8908871 Raynaud's phenomenon
89088716 8908871 Rib fracture
89088716 8908871 Stress fracture
89088716 8908871 Surgery
89088716 8908871 Tibia fracture
89088716 8908871 Urinary incontinence
89088716 8908871 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
89088716 8908871 1 20030820 20031202 0
89088716 8908871 2 200606 0
89088716 8908871 3 20041209 20060501 0
89088716 8908871 4 1998 0
89088716 8908871 5 20030908 2006 0
89088716 8908871 6 20030908 2006 0
89088716 8908871 7 20030908 2006 0
89088716 8908871 8 20030908 2006 0
89088716 8908871 9 20061006 0
89088716 8908871 10 20030908 200606 0