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
126201801 12620180 1 I 19891223 20160727 20160803 20160803 EXP DE-ALLERGAN-1664590US ALLERGAN 68.00 YR M Y 80.00000 KG 20160803 MD COUNTRY NOT SPECIFIED DE

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
126201801 12620180 1 PS SUCRALFATE - BP SUCRALFATE 1 Oral 4 DF, QD 84 DF Y U 19183 4 DF QD
126201801 12620180 2 SS SUCRALFATE - BP SUCRALFATE 1 84 DF Y U 19183
126201801 12620180 3 SS PIROXICAM. PIROXICAM 1 Oral 20 MG, QD U U 0 20 MG QD
126201801 12620180 4 SS ACETYLSALICYLIC ACID ASPIRIN 1 Oral 1.5 MG, QD U U 0 1.5 MG QD
126201801 12620180 5 C BELOC METOPROLOL TARTRATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126201801 12620180 1 Gastritis
126201801 12620180 2 Duodenitis
126201801 12620180 3 Dislocation of vertebra
126201801 12620180 4 Cerebrovascular disorder
126201801 12620180 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126201801 12620180 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126201801 12620180 Upper gastrointestinal haemorrhage

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
126201801 12620180 1 19891203 19891223 0
126201801 12620180 5 1980 0