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
125023472 12502347 2 F 2016 20160627 20160627 20160706 EXP CA-GILEAD-2016-0220464 GILEAD 63.00 YR A F Y 72.00000 KG 20160706 OT CA CA

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
125023472 12502347 1 PS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, UNK 205834 1 DF TABLET
125023472 12502347 2 I AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 250 MG, UNK Y 0 250 MG
125023472 12502347 3 I AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Y 0
125023472 12502347 4 SS AMOXICILLIN. AMOXICILLIN 1 Oral 500 MG, UNK Y 0 500 MG
125023472 12502347 5 SS AMOXICILLIN. AMOXICILLIN 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125023472 12502347 1 Hepatitis C
125023472 12502347 2 Pharyngitis
125023472 12502347 3 Bronchitis
125023472 12502347 4 Pharyngitis
125023472 12502347 5 Bronchitis

Outcome of event

Event ID CASEID OUTC COD
125023472 12502347 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125023472 12502347 Ascites
125023472 12502347 Bronchitis
125023472 12502347 Drug interaction
125023472 12502347 Drug-induced liver injury
125023472 12502347 Hyperbilirubinaemia
125023472 12502347 Malaise
125023472 12502347 Pharyngitis
125023472 12502347 Pyrexia

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
125023472 12502347 1 20160304 0
125023472 12502347 2 20160608 20160613 0
125023472 12502347 4 20160601 20160604 0