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
108820767 10882076 7 F 2007 20160815 20150303 20160821 EXP US-009507513-1109USA00853 MERCK 0.00 F Y 81.63000 KG 20160821 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
108820767 10882076 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QD 20560 70 MG TABLET QD
108820767 10882076 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70MG 20560 70 MG TABLET
108820767 10882076 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108820767 10882076 1 Osteoporosis
108820767 10882076 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
108820767 10882076 OT
108820767 10882076 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108820767 10882076 Abscess oral
108820767 10882076 Amalgam tattoo
108820767 10882076 Amnesia
108820767 10882076 Anaemia
108820767 10882076 Anxiety
108820767 10882076 Aortic calcification
108820767 10882076 Arthralgia
108820767 10882076 Arthritis
108820767 10882076 Back pain
108820767 10882076 Body height decreased
108820767 10882076 Bone density decreased
108820767 10882076 Bone disorder
108820767 10882076 Bursitis
108820767 10882076 Dental caries
108820767 10882076 Depression
108820767 10882076 Drug ineffective
108820767 10882076 Femur fracture
108820767 10882076 Fibromyalgia
108820767 10882076 Fracture
108820767 10882076 Gingivitis
108820767 10882076 Hypercholesterolaemia
108820767 10882076 Hyperparathyroidism
108820767 10882076 Hypertension
108820767 10882076 Hypertrophy
108820767 10882076 Immunology test abnormal
108820767 10882076 Inappropriate schedule of drug administration
108820767 10882076 Intervertebral disc degeneration
108820767 10882076 Intramedullary rod insertion
108820767 10882076 Loose tooth
108820767 10882076 Lumbar radiculopathy
108820767 10882076 Macular degeneration
108820767 10882076 Mixed connective tissue disease
108820767 10882076 Muscle spasms
108820767 10882076 Muscular weakness
108820767 10882076 Myalgia
108820767 10882076 Myositis
108820767 10882076 Nausea
108820767 10882076 Oedema peripheral
108820767 10882076 Osteoarthritis
108820767 10882076 Osteomyelitis
108820767 10882076 Osteonecrosis of jaw
108820767 10882076 Osteopenia
108820767 10882076 Pain
108820767 10882076 Palatal disorder
108820767 10882076 Periodontitis
108820767 10882076 Polyarthritis
108820767 10882076 Raynaud's phenomenon
108820767 10882076 Scoliosis
108820767 10882076 Sjogren's syndrome
108820767 10882076 Spinal osteoarthritis
108820767 10882076 Spinal pain
108820767 10882076 Stress fracture
108820767 10882076 Tooth disorder
108820767 10882076 Traumatic occlusion
108820767 10882076 Undifferentiated connective tissue disease
108820767 10882076 Urticaria
108820767 10882076 Vertigo positional
108820767 10882076 Vitamin D deficiency
108820767 10882076 Vomiting

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
108820767 10882076 2 20070824 20101109 0
108820767 10882076 3 20090615 201010 0