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
127116721 12711672 1 I 20160810 20160822 20160902 20160902 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123047 RANBAXY 43.00 YR F Y 110.67000 KG 20160902 OT GB GB

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
127116721 12711672 1 PS LORATADINE. LORATADINE 1 Unknown UNK U U 76134
127116721 12711672 2 SS FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown UNK U U 0
127116721 12711672 3 SS DAKTARIN MICONAZOLE NITRATE 1 Oral 2.5 ML, QID 10 ML Y U GAB0Y00 0 2.5 ML Q6H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127116721 12711672 1 Seasonal allergy
127116721 12711672 2 Anxiety
127116721 12711672 3 Oral candidiasis

Outcome of event

Event ID CASEID OUTC COD
127116721 12711672 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127116721 12711672 Diarrhoea
127116721 12711672 Drug interaction

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
127116721 12711672 3 20160810 20160811 0