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
126253282 12625328 2 F 20160809 20160805 20160822 EXP TR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121453 RANBAXY 74.00 YR F Y 0.00000 20160822 OT GB TR

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
126253282 12625328 1 PS LITHIUM. LITHIUM 1 Oral 300 MG, TID Y U 91027 300 MG Q8H
126253282 12625328 2 I QUETIAPINE. QUETIAPINE 1 Unknown 400 MG, DAILY Y U 0 400 MG
126253282 12625328 3 I Valsartan/Hydrochlorothiazide HYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown 160 MG/ 25 MG ONCE DAILY Y U 0
126253282 12625328 4 C LEVODOPA/CARBIDOPA 250/25 2 Unknown 1 DF, BID Y U 0 1 DF Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126253282 12625328 1 Product used for unknown indication
126253282 12625328 2 Product used for unknown indication
126253282 12625328 3 Product used for unknown indication
126253282 12625328 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126253282 12625328 HO
126253282 12625328 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126253282 12625328 Blood pressure increased
126253282 12625328 Coma scale abnormal
126253282 12625328 Confusional state
126253282 12625328 Drug interaction
126253282 12625328 Mental disorder
126253282 12625328 Muscle rigidity
126253282 12625328 Nausea
126253282 12625328 Stupor
126253282 12625328 Toxicity to various agents
126253282 12625328 Vomiting

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

no results found

Therapies reported

no results found