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
125577681 12557768 1 I 20160701 20160714 20160714 EXP TR-ELI_LILLY_AND_COMPANY-TR201607004451 ELI LILLY AND CO 5.00 YR M Y 0.00000 20160713 CN 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
125577681 12557768 1 PS OLANZAPINE. OLANZAPINE 1 Oral Y U 20592

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125577681 12557768 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125577681 12557768 OT
125577681 12557768 HO
125577681 12557768 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125577681 12557768 Coma scale abnormal
125577681 12557768 Depressed level of consciousness
125577681 12557768 Hypertonia
125577681 12557768 Hypocalcaemia
125577681 12557768 Hypomagnesaemia
125577681 12557768 Hypotension
125577681 12557768 Leukopenia
125577681 12557768 Miosis
125577681 12557768 Respiratory rate decreased
125577681 12557768 Tonic convulsion
125577681 12557768 Toxicity to various agents
125577681 12557768 Unresponsive to stimuli

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

no results found

Therapies reported

no results found