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
127768601 12776860 1 I 201412 20150203 20160923 20160923 EXP US-GILEAD-2015-0135977 GILEAD 62.00 YR A M Y 0.00000 20160923 CN US 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
127768601 12776860 1 PS SOFOSBUVIR SOFOSBUVIR 1 Oral 400 MG, UNK U 204671 400 MG TABLET
127768601 12776860 2 SS SOFOSBUVIR SOFOSBUVIR 1 Oral 400 UNK, UNK U 204671 400 MG TABLET
127768601 12776860 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNK D 0
127768601 12776860 4 SS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127768601 12776860 1 Chronic hepatitis C
127768601 12776860 3 Chronic hepatitis C
127768601 12776860 4 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127768601 12776860 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127768601 12776860 Affective disorder
127768601 12776860 Anxiety
127768601 12776860 Crohn's disease
127768601 12776860 Drug ineffective
127768601 12776860 Hepatitis C
127768601 12776860 Irritability
127768601 12776860 Restlessness

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
127768601 12776860 1 20140702 20140923 0
127768601 12776860 2 2015 2015 0
127768601 12776860 3 20140702 20140923 0
127768601 12776860 4 20140702 20140923 0