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
124827042 12482704 2 F 20160501 20160727 20160620 20160805 EXP PHEH2016US015025 NOVARTIS 54.48 YR M Y 86.45000 KG 20160805 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
124827042 12482704 1 PS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 50 MG, QD 22291 50 MG TABLET QD
124827042 12482704 2 C ELAVIL AMITRIPTYLINE HYDROCHLORIDE 1 Oral UNK, QD (IN TH EVENING) U 0 5 MG TABLET QD
124827042 12482704 3 C SOFOSBUVIR SOFOSBUVIR 1 Unknown UNK U 0
124827042 12482704 4 C RIBAVIRIN. RIBAVIRIN 1 Unknown 800 MG, QD U 0 800 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124827042 12482704 1 Thrombocytopenia
124827042 12482704 2 Product used for unknown indication
124827042 12482704 3 Hepatitis C
124827042 12482704 4 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
124827042 12482704 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124827042 12482704 Epistaxis
124827042 12482704 Fatigue
124827042 12482704 General physical health deterioration
124827042 12482704 Pain
124827042 12482704 Platelet 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
124827042 12482704 1 20121206 20160512 0
124827042 12482704 3 20140228 0
124827042 12482704 4 20140228 0