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
126926871 12692687 1 I 20160319 20160816 20160829 20160829 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122733 RANBAXY 34.00 YR F Y 0.00000 20160829 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
126926871 12692687 1 SS CLOTRIMAZOLE. CLOTRIMAZOLE 1 Unknown 500 MG, USED APPROXIMATELY 3 TIMES U U 0 500 MG
126926871 12692687 2 SS CANESTEN CLOTRIMAZOLE 1 Vaginal 2 DF, ONCE U U BXH9NG2 0 2 DF
126926871 12692687 3 PS FLUCONAZOLE. FLUCONAZOLE 1 Unknown 150 MG, ONCE U U 76332 150 MG
126926871 12692687 4 SS FLUCONAZOLE. FLUCONAZOLE 1 Unknown 150 MG, ONCE U U 76332 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126926871 12692687 1 Vulvovaginal candidiasis
126926871 12692687 2 Vulvovaginal candidiasis
126926871 12692687 3 Vulvovaginal candidiasis

Outcome of event

Event ID CASEID OUTC COD
126926871 12692687 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126926871 12692687 Asthenia
126926871 12692687 Chest pain
126926871 12692687 Drug hypersensitivity
126926871 12692687 Drug ineffective
126926871 12692687 Dyspnoea
126926871 12692687 Laryngotracheal oedema
126926871 12692687 Product use issue
126926871 12692687 Swollen tongue

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
126926871 12692687 1 201511 201601 0
126926871 12692687 2 20160319 20160320 0
126926871 12692687 3 201601 201601 0
126926871 12692687 4 201604 201604 0