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
125318922 12531892 2 F 20160321 20160722 20160706 20160722 EXP 2016-000863 WARNER CHILCOTT WARNER CHILCOTT 87.00 YR F Y 0.00000 20160722 MD JP JP

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
125318922 12531892 1 PS ACTONEL RISEDRONATE SODIUM 1 Oral Y 20835 75 MG TABLET
125318922 12531892 2 C BROMELAIN BROMELAINS 1 0
125318922 12531892 3 C TOCOPHEROL ACETATE .ALPHA.-TOCOPHEROL ACETATE 1 0
125318922 12531892 4 C MAGMITT MAGNESIUM OXIDE 1 0
125318922 12531892 5 C BORRAZA-G LIDOCAINETRIBENOSIDE 1 0
125318922 12531892 6 C LOXOPROFEN SODIUM LOXOPROFEN SODIUM 1 Y 0
125318922 12531892 7 C FAMOTIDINE. FAMOTIDINE 1 Y 0
125318922 12531892 8 C NORVASC AMLODIPINE BESYLATE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125318922 12531892 HO
125318922 12531892 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125318922 12531892 Blood creatine phosphokinase increased
125318922 12531892 Blood potassium decreased
125318922 12531892 C-reactive protein increased
125318922 12531892 Fall
125318922 12531892 Myositis
125318922 12531892 Pain
125318922 12531892 Painful respiration

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
125318922 12531892 1 20160320 2016 0
125318922 12531892 2 20100910 0
125318922 12531892 4 20100910 0
125318922 12531892 5 20100910 0
125318922 12531892 6 20160323 0
125318922 12531892 7 20160323 0