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
101816416 10181641 6 F 2009 20160901 20140519 20160908 EXP US-009507513-1405USA004513 MERCK 0.00 F Y 0.00000 20160908 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
101816416 10181641 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
101816416 10181641 2 SS FOSAMAX ALENDRONATE SODIUM 1 U 20560 TABLET
101816416 10181641 3 SS ZOMETA ZOLEDRONIC ACID 1 Unknown 4 MG, EACH MONTH U 0 4 MG /month
101816416 10181641 4 C CALCIUM (UNSPECIFIED) CALCIUM 1 Unknown 1200 MG, QD U 0 1200 MG QD
101816416 10181641 5 C ASCORBIC ACID. ASCORBIC ACID 1 Unknown 2000 MG, QD U 0 2000 MG QD
101816416 10181641 6 C VITAMIN D CHOLECALCIFEROL 1 Oral 1000 IU, QD U 0 1000 IU QD
101816416 10181641 7 C VITAMIN E .ALPHA.-TOCOPHEROL 1 Unknown 500 MG, QD U 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101816416 10181641 1 Osteopenia
101816416 10181641 2 Osteoporosis
101816416 10181641 3 Osteoporosis
101816416 10181641 4 Product used for unknown indication
101816416 10181641 5 Product used for unknown indication
101816416 10181641 6 Product used for unknown indication
101816416 10181641 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101816416 10181641 OT
101816416 10181641 HO
101816416 10181641 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
101816416 10181641 Acute kidney injury
101816416 10181641 Anaemia
101816416 10181641 Asthenia
101816416 10181641 Bone marrow transplant
101816416 10181641 Breast cancer metastatic
101816416 10181641 Breast neoplasm
101816416 10181641 Confusional state
101816416 10181641 Coombs test positive
101816416 10181641 Deep vein thrombosis
101816416 10181641 Diverticulum
101816416 10181641 Dizziness
101816416 10181641 Dizziness postural
101816416 10181641 Encephalopathy
101816416 10181641 Fall
101816416 10181641 Fatigue
101816416 10181641 Femur fracture
101816416 10181641 Foot fracture
101816416 10181641 Haemarthrosis
101816416 10181641 Haemoglobin decreased
101816416 10181641 Hepatic lesion
101816416 10181641 Hepatitis acute
101816416 10181641 Hypertension
101816416 10181641 Joint effusion
101816416 10181641 Lymphadenectomy
101816416 10181641 Mastectomy
101816416 10181641 Metastases to liver
101816416 10181641 Oedema
101816416 10181641 Osteoporosis
101816416 10181641 Renal cyst
101816416 10181641 Solar lentigo
101816416 10181641 Subarachnoid haemorrhage
101816416 10181641 Thrombocytopenia
101816416 10181641 Thrombotic thrombocytopenic purpura
101816416 10181641 Urinary tract infection

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
101816416 10181641 1 199911 200902 0
101816416 10181641 3 200903 0
101816416 10181641 4 200001 0
101816416 10181641 5 200001 0
101816416 10181641 6 200001 0
101816416 10181641 7 200001 0