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
110375754 11037575 4 F 20160624 20150416 20160708 EXP NZ-SUN PHARMACEUTICAL INDUSTRIES LTD-2015R1-95706 RANBAXY 55.00 YR F Y 0.00000 20160708 MD NZ NZ

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
110375754 11037575 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown UNK U 77032
110375754 11037575 2 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 900 ?G, 1/WEEK U 0 900 UG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110375754 11037575 1 Product used for unknown indication
110375754 11037575 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
110375754 11037575 OT
110375754 11037575 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
110375754 11037575 Confusional state
110375754 11037575 Depressed level of consciousness
110375754 11037575 Dizziness
110375754 11037575 Generalised tonic-clonic seizure
110375754 11037575 Hyperreflexia
110375754 11037575 Intentional overdose
110375754 11037575 Nystagmus
110375754 11037575 Vomiting

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

no results found

Therapies reported

no results found