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
1087187910 10871879 10 F 2006 20160815 20150226 20160824 EXP US-009507513-1109USA00855 MERCK 0.00 F Y 0.00000 20160824 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
1087187910 10871879 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
1087187910 10871879 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
1087187910 10871879 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 0 70 MG /wk
1087187910 10871879 4 SS ACTONEL RISEDRONATE SODIUM 1 Oral UNK UNK, UNKNOWN 0
1087187910 10871879 5 C VITAMIN D CHOLECALCIFEROL 1 Oral 400 IU, QD 0 400 IU QD
1087187910 10871879 6 C ASCORBIC ACID. ASCORBIC ACID 1 Oral 500 MG, QD 0 500 MG QD
1087187910 10871879 7 C CYANOCOBALAMIN. CYANOCOBALAMIN 1 1000 MG, QD 0 1000 MG QD
1087187910 10871879 8 C CALCIUM (UNSPECIFIED) CALCIUM 1 Unknown 1000 MG, QD 0 1000 MG QD
1087187910 10871879 9 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown UNK, UNKNOWN 0
1087187910 10871879 10 C CYTOSPORT CYTOMAX 2 Unknown UNK, UNKNOWN 0
1087187910 10871879 11 C LIOTHYRONINE SODIUM. LIOTHYRONINE SODIUM 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1087187910 10871879 1 Osteopenia
1087187910 10871879 2 Osteopenia
1087187910 10871879 3 Osteopenia
1087187910 10871879 4 Osteopenia
1087187910 10871879 5 Vitamin supplementation
1087187910 10871879 6 Vitamin supplementation
1087187910 10871879 7 Vitamin supplementation
1087187910 10871879 8 Vitamin supplementation
1087187910 10871879 9 Product used for unknown indication
1087187910 10871879 10 Product used for unknown indication
1087187910 10871879 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1087187910 10871879 HO
1087187910 10871879 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1087187910 10871879 Arthralgia
1087187910 10871879 Autoimmune thyroiditis
1087187910 10871879 Calcium deficiency
1087187910 10871879 Drug hypersensitivity
1087187910 10871879 Fall
1087187910 10871879 Femur fracture
1087187910 10871879 Groin pain
1087187910 10871879 Hypercholesterolaemia
1087187910 10871879 Hypoaesthesia
1087187910 10871879 Hypothyroidism
1087187910 10871879 Impaired healing
1087187910 10871879 Intramedullary rod insertion
1087187910 10871879 Laceration
1087187910 10871879 Medical device removal
1087187910 10871879 Oedema
1087187910 10871879 Pruritus
1087187910 10871879 Seasonal allergy
1087187910 10871879 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
1087187910 10871879 1 200405 200804 0
1087187910 10871879 2 200803 200806 0
1087187910 10871879 3 200806 201108 0
1087187910 10871879 4 2002 200404 0
1087187910 10871879 5 2001 0
1087187910 10871879 6 2001 0
1087187910 10871879 7 2001 0
1087187910 10871879 8 2001 0
1087187910 10871879 9 2003 0
1087187910 10871879 10 2003 0
1087187910 10871879 11 2003 0