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
127397221 12739722 1 I 20160513 20160907 20160913 20160913 EXP GB-MHRA-TPP6358628C1231474YC1472415908781 GB-MYLANLABS-2016M1038108 MYLAN 0.00 Y 0.00000 20160913 MD 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
127397221 12739722 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 UNK U U 65195
127397221 12739722 2 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 1 DF, QD (EACH MORNING) 330 DF U 0 1 DF QD
127397221 12739722 3 C BETAMETHASONE VALERATE. BETAMETHASONE VALERATE 1 1 DF, BID 80 DF U 0 1 DF BID
127397221 12739722 4 C LERCANIDIPINE HYDROCHLORIDE LERCANIDIPINE HYDROCHLORIDE 1 1 DF, QD 330 DF U 0 1 DF QD
127397221 12739722 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 1 DF, BID 660 DF U 0 1 DF BID
127397221 12739722 6 C RAMIPRIL. RAMIPRIL 1 1 DF, QD 330 DF U 0 1 DF QD
127397221 12739722 7 C SIMVASTATIN. SIMVASTATIN 1 1 DF, QD (NOCTE) 330 DF U 0 1 DF QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127397221 12739722 OT
127397221 12739722 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127397221 12739722 Burning sensation
127397221 12739722 Rash

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
127397221 12739722 1 20160513 0
127397221 12739722 2 20150618 0
127397221 12739722 3 20160622 20160702 0
127397221 12739722 4 20150618 0
127397221 12739722 5 20150618 0
127397221 12739722 6 20150618 0
127397221 12739722 7 20150618 0