The Safety Rates Drug Report

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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
126033191 12603319 1 I 20160711 20160719 20160728 20160728 EXP GB-MHRA-TPP4141954C2099707YC1468258667115 GB-WATSON-2016-16159 WATSON 53.00 YR F Y 66.00000 KG 20160728 CN GB GB

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
126033191 12603319 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U UNCONFIRMED 77671 UNK
126033191 12603319 2 C INDAPAMIDE. INDAPAMIDE 1 Unknown 1 DF, QAM (EACH MORNING) 1 DF U 0 1 DF QD
126033191 12603319 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown 1 DF, DAILY - TO PROTECT THE STOMACH. 187.957993 DF U 0 1 DF QD
126033191 12603319 4 C RAMIPRIL. RAMIPRIL 1 Unknown 1 DF, DAILY 187.957993 DF U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126033191 12603319 1 Product used for unknown indication
126033191 12603319 2 Product used for unknown indication
126033191 12603319 3 Prophylaxis
126033191 12603319 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126033191 12603319 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126033191 12603319 Fatigue
126033191 12603319 Joint swelling

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
126033191 12603319 1 20160628 0
126033191 12603319 2 20160711 0
126033191 12603319 3 20160105 0
126033191 12603319 4 20160105 0