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
126472822 12647282 2 F 20160902 20160812 20160915 EXP NL-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-121851 RANBAXY 43.00 YR M Y 0.00000 20160915 OT GB NL

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
126472822 12647282 1 PS QUETIAPINE. QUETIAPINE 1 Oral 13 G 201190 TABLET
126472822 12647282 2 SS VALPROIC ACID. VALPROIC ACID 1 Oral 45 G U 0 PROLONGED-RELEASE TABLET
126472822 12647282 3 SS OXAZEPAM. OXAZEPAM 1 Oral 1.1 GRAM 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126472822 12647282 1 Product used for unknown indication
126472822 12647282 2 Product used for unknown indication
126472822 12647282 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126472822 12647282 HO
126472822 12647282 LT
126472822 12647282 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126472822 12647282 Blood creatine phosphokinase increased
126472822 12647282 Coma
126472822 12647282 Electrocardiogram QT prolonged
126472822 12647282 Haemodynamic instability
126472822 12647282 Hepatic function abnormal
126472822 12647282 Hyperammonaemia
126472822 12647282 Intentional overdose
126472822 12647282 Toxicity to various agents

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

no results found

Therapies reported

no results found