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
125471342 12547134 2 F 20160715 20160711 20160721 EXP US-ABBVIE-16P-163-1669988-00 ABBVIE 0.00 M Y 70.37000 KG 20160721 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
125471342 12547134 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral PER DIRECTIONS ON PACKAGE UNKNOWN 206619 TABLET BID
125471342 12547134 2 SS MEGACE MEGESTROL ACETATE 1 Unknown U 0
125471342 12547134 3 C XANAX ALPRAZOLAM 1 0 .25 MG
125471342 12547134 4 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0 100 MG
125471342 12547134 5 C CYPROHEPTADINE. CYPROHEPTADINE 1 0
125471342 12547134 6 C LORAZEPAM. LORAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125471342 12547134 1 Hepatitis C
125471342 12547134 2 Decreased appetite
125471342 12547134 3 Product used for unknown indication
125471342 12547134 4 Depression
125471342 12547134 5 Product used for unknown indication
125471342 12547134 6 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125471342 12547134 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125471342 12547134 Asthenia
125471342 12547134 Decreased appetite
125471342 12547134 Malaise
125471342 12547134 Mental disorder
125471342 12547134 Nausea
125471342 12547134 Pain
125471342 12547134 Rash papular
125471342 12547134 Weight decreased
125471342 12547134 White blood cell count increased

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
125471342 12547134 1 20160604 0