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
127407132 12740713 2 F 20160831 20160914 20160914 EXP DE-CIPLA LTD.-2016DE18027 CIPLA 0.00 Y 0.00000 20160914 OT DE 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
127407132 12740713 1 I AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U U 0
127407132 12740713 2 PS RITONAVIR. RITONAVIR 1 Oral UNK U U 203759
127407132 12740713 3 I Sofosbuvir SOFOSBUVIR 1 Oral UNK U U 0
127407132 12740713 4 I Sofosbuvir + Ledipasvir LEDIPASVIRSOFOSBUVIR 1 Oral UNK U U 0
127407132 12740713 5 I Simeprevir SIMEPREVIR 1 Oral UNK U U 0
127407132 12740713 6 I DACLATASVIR. DACLATASVIR 1 Oral UNK U U 0
127407132 12740713 7 I Ombitasvir OMBITASVIR 1 Oral UNK U U 0
127407132 12740713 8 I PARATAPREVIR PARITAPREVIR 1 Oral UNK U U 0
127407132 12740713 9 I Dasabuvir DASABUVIR 1 Oral UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127407132 12740713 2 Hepatitis C
127407132 12740713 3 Hepatitis C
127407132 12740713 4 Hepatitis C
127407132 12740713 5 Hepatitis C
127407132 12740713 6 Hepatitis C
127407132 12740713 7 Hepatitis C
127407132 12740713 8 Hepatitis C
127407132 12740713 9 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127407132 12740713 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127407132 12740713 Drug interaction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found