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
125088592 12508859 2 F 201605 20160714 20160629 20160719 EXP GB-MHRA-EYC 00141303 GB-PFIZER INC-2016317521 PFIZER 60.00 YR M Y 117.00000 KG 20160719 OT 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
125088592 12508859 1 PS SERTRALINE HCL SERTRALINE HYDROCHLORIDE 1 Oral 100 MG, UNK 19839 100 MG
125088592 12508859 2 I HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, (DOSE AND FREQUENCY UNSPECIFIED) 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125088592 12508859 1 Depression
125088592 12508859 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125088592 12508859 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125088592 12508859 Anxiety
125088592 12508859 Cold sweat
125088592 12508859 Condition aggravated
125088592 12508859 Drug interaction

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
125088592 12508859 1 2014 0
125088592 12508859 2 201603 0