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
127407261 12740726 1 I 20160831 20160914 20160914 EXP DE-CIPLA LTD.-2016DE18029 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
127407261 12740726 1 PS RITONAVIR. RITONAVIR 1 Oral UNK U U 0
127407261 12740726 2 SS CARVEDILOL. CARVEDILOL 1 Unknown UNK U U 0
127407261 12740726 3 I Sofosbuvir + Ledipasvir LEDIPASVIRSOFOSBUVIR 1 Oral UNK U U 0
127407261 12740726 4 I Sofosbuvir SOFOSBUVIR 1 Oral UNK U U 0
127407261 12740726 5 I DACLATASVIR. DACLATASVIR 1 Oral UNK U U 0
127407261 12740726 6 I Dasabuvir DASABUVIR 1 Oral UNK U U 0
127407261 12740726 7 I PARATAPREVIR PARITAPREVIR 1 Oral UNK U U 0
127407261 12740726 8 I Ombitasvir OMBITASVIR 1 Oral UNK U U 0
127407261 12740726 9 I RIBAVIRIN. RIBAVIRIN 1 Oral UNK U U 0
127407261 12740726 10 I Simeprevir SIMEPREVIR 1 Oral UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127407261 12740726 1 Hepatitis C
127407261 12740726 3 Hepatitis C
127407261 12740726 4 Hepatitis C
127407261 12740726 5 Hepatitis C
127407261 12740726 6 Hepatitis C
127407261 12740726 7 Hepatitis C
127407261 12740726 8 Hepatitis C
127407261 12740726 9 Hepatitis C
127407261 12740726 10 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127407261 12740726 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127407261 12740726 Drug interaction

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

no results found

Therapies reported

no results found