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
126464682 12646468 2 F 20160302 20160808 20160812 20160817 EXP JP-009507513-1608JPN004914 MERCK 71.00 YR M Y 55.00000 KG 20160817 MD JP JP

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
126464682 12646468 1 PS REBETOL RIBAVIRIN 1 Oral 600 MG, QD 50400 MG U 20903 600 MG CAPSULE QD
126464682 12646468 2 SS SOVALDI SOFOSBUVIR 1 Oral 400 MG, QD 33600 MG U 0 400 MG TABLET QD
126464682 12646468 3 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 Oral 0
126464682 12646468 4 C GLIMEPIRIDE. GLIMEPIRIDE 1 Oral 0
126464682 12646468 5 C NESINA ALOGLIPTIN BENZOATE 1 Oral 0
126464682 12646468 6 C ALLOPURINOL. ALLOPURINOL 1 Oral UNK 0
126464682 12646468 7 C URALYT (potassium citrate (+) sodium citrate) 2 Oral UNK 0
126464682 12646468 8 C BROTIZOLAM BROTIZOLAM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126464682 12646468 3 Hypertension
126464682 12646468 4 Diabetes mellitus
126464682 12646468 5 Diabetes mellitus
126464682 12646468 6 Hyperuricaemia
126464682 12646468 7 Calculus urinary
126464682 12646468 8 Insomnia

Outcome of event

Event ID CASEID OUTC COD
126464682 12646468 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126464682 12646468 Hepatocellular carcinoma

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
126464682 12646468 1 20151208 20160229 0
126464682 12646468 2 20151208 20160229 0