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
125506242 12550624 2 F 201604 20160715 20160712 20160720 EXP US-ABBVIE-16P-163-1670509-00 ABBVIE 60.49 YR F Y 81.72000 KG 20160720 CN COUNTRY NOT SPECIFIED US

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
125506242 12550624 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 1047736 206619 TABLET BID
125506242 12550624 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0 600 MG TABLET QOD
125506242 12550624 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0 400 MG TABLET QOD
125506242 12550624 4 C LISINOPRIL. LISINOPRIL 1 0
125506242 12550624 5 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
125506242 12550624 6 C AMBIEN ZOLPIDEM TARTRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125506242 12550624 1 Hepatitis C
125506242 12550624 2 Hepatitis C
125506242 12550624 4 Hypertension
125506242 12550624 5 Dyspepsia
125506242 12550624 6 Insomnia

Outcome of event

Event ID CASEID OUTC COD
125506242 12550624 HO
125506242 12550624 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125506242 12550624 Anaemia
125506242 12550624 Asthenia
125506242 12550624 Diarrhoea
125506242 12550624 Diverticulitis
125506242 12550624 Haemoglobin decreased
125506242 12550624 Sluggishness
125506242 12550624 Vomiting
125506242 12550624 White blood cell count decreased

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
125506242 12550624 1 20160404 0
125506242 12550624 2 20160404 20160706 0
125506242 12550624 3 20160706 0