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
79503868 7950386 8 F 200109 20160803 20110518 20160808 EXP US-009507513-1105USA02547 MERCK 0.00 F Y 54.43000 KG 20160808 OT 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
79503868 7950386 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
79503868 7950386 2 SS FOSAMAX ALENDRONATE SODIUM 1 U 20560 TABLET
79503868 7950386 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Unknown UNK 20560 TABLET
79503868 7950386 4 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 0 70 MG
79503868 7950386 5 C CALCIUM (UNSPECIFIED) CALCIUM 1 UNK MG, UNK 0
79503868 7950386 6 C VITAMIN D CHOLECALCIFEROL 1 UNK MG, UNK 0
79503868 7950386 7 C LEVOTIROXINA S.O LEVOTHYROXINE 1 UNK MG, UNK 0 TABLET
79503868 7950386 8 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK MG, UNK 0 CAPSULE
79503868 7950386 9 C EVISTA RALOXIFENE HYDROCHLORIDE 1 UNK MG, UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79503868 7950386 1 Osteoporosis
79503868 7950386 2 Osteopenia
79503868 7950386 3 Prophylaxis
79503868 7950386 4 Osteoporosis
79503868 7950386 7 Hypothyroidism
79503868 7950386 8 Gastrooesophageal reflux disease
79503868 7950386 9 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
79503868 7950386 OT
79503868 7950386 DS
79503868 7950386 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
79503868 7950386 Adverse drug reaction
79503868 7950386 Anxiety
79503868 7950386 Back pain
79503868 7950386 Blood potassium decreased
79503868 7950386 Blood pressure decreased
79503868 7950386 Blood urea increased
79503868 7950386 Bradycardia
79503868 7950386 Cerebral atrophy
79503868 7950386 Cerebrovascular accident
79503868 7950386 Chronic kidney disease
79503868 7950386 Chronic obstructive pulmonary disease
79503868 7950386 Craniocerebral injury
79503868 7950386 Cystocele
79503868 7950386 Depression
79503868 7950386 Fall
79503868 7950386 Fracture
79503868 7950386 Gait disturbance
79503868 7950386 Haemorrhage
79503868 7950386 Hiatus hernia
79503868 7950386 Hip fracture
79503868 7950386 Hyperlipidaemia
79503868 7950386 Hypertension
79503868 7950386 Hypoacusis
79503868 7950386 Hyponatraemia
79503868 7950386 Hypotension
79503868 7950386 Impaired healing
79503868 7950386 Incorrect dose administered
79503868 7950386 Intervertebral disc protrusion
79503868 7950386 Laceration
79503868 7950386 Leukocytosis
79503868 7950386 Loss of consciousness
79503868 7950386 Low turnover osteopathy
79503868 7950386 Multiple sclerosis
79503868 7950386 Musculoskeletal chest pain
79503868 7950386 Oral disorder
79503868 7950386 Osteoarthritis
79503868 7950386 Pelvic deformity
79503868 7950386 Peripheral vascular disorder
79503868 7950386 Pulmonary mass
79503868 7950386 Pyrexia
79503868 7950386 Radius fracture
79503868 7950386 Rib fracture
79503868 7950386 Sciatica
79503868 7950386 Spinal column stenosis
79503868 7950386 Spinal osteoarthritis
79503868 7950386 Syncope
79503868 7950386 Tooth disorder
79503868 7950386 Urinary tract infection
79503868 7950386 Uterine leiomyoma
79503868 7950386 Wrist fracture

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
79503868 7950386 1 1995 2009 0
79503868 7950386 3 200901 200905 0
79503868 7950386 4 20020301 200910 0
79503868 7950386 5 1998 0
79503868 7950386 6 1998 0
79503868 7950386 7 1984 0
79503868 7950386 8 1995 0
79503868 7950386 9 1995 0