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
127069261 12706926 1 I 20160715 20160819 20160901 20160901 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122942 RANBAXY 86.98 YR M Y 0.00000 20160901 OT IT IT

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
127069261 12706926 1 PS LEVETIRACETAM. LEVETIRACETAM 1 Unknown 1000 MG DAILY U U 203059 1000 MG
127069261 12706926 2 C DEURSIL 300 MG 2 Unknown UNK U U 0
127069261 12706926 3 C FOLINA 5 MG 2 Unknown U U 0
127069261 12706926 4 C TARCEVA 100 MG 2 Unknown U U 0
127069261 12706926 5 C TIKLID 250 MG TICLOPIDINE HYDROCHLORIDE 1 Unknown U U 0
127069261 12706926 6 C ESOMEPRAZOLE SODIUM. ESOMEPRAZOLE SODIUM 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127069261 12706926 1 Petit mal epilepsy
127069261 12706926 2 Product used for unknown indication
127069261 12706926 3 Product used for unknown indication
127069261 12706926 4 Product used for unknown indication
127069261 12706926 5 Product used for unknown indication
127069261 12706926 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127069261 12706926 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127069261 12706926 Irritability
127069261 12706926 Product substitution issue
127069261 12706926 Somnolence

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
127069261 12706926 1 20160715 20160730 0