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
127985671 12798567 1 I 20160919 20160930 20160930 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-125120 RANBAXY 26.00 YR M Y 0.00000 20160930 OT GB 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
127985671 12798567 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown UNK 65174
127985671 12798567 2 C FLUCONAZOLE. FLUCONAZOLE 1 Intravenous (not otherwise specified) 400 MG, BID U 0 400 MG Q12H
127985671 12798567 3 C FLUCYTOSINE. FLUCYTOSINE 1 Unknown 2000 MG, BID U 0 2000 MG Q12H
127985671 12798567 4 C Pentamidine PENTAMIDINE 1 Unknown 4 MG/KG, DAILY U 0 4 MG/KG
127985671 12798567 5 C PHENYTOIN. PHENYTOIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127985671 12798567 1 Amoebic brain abscess
127985671 12798567 2 Amoebic brain abscess
127985671 12798567 3 Amoebic brain abscess
127985671 12798567 4 Amoebic brain abscess
127985671 12798567 5 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127985671 12798567 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127985671 12798567 Atrial fibrillation
127985671 12798567 Cardiotoxicity
127985671 12798567 Electrocardiogram QT prolonged

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found