The Safety Rates Drug Report

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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
125944361 12594436 1 I 20160602 20160726 20160726 PER US-ASTRAZENECA-2016SE60727 ASTRAZENECA 0.00 F Y 0.00000 20160726 CN US US

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
125944361 12594436 1 PS SEROQUEL QUETIAPINE FUMARATE 1 Oral U 20639 TABLET
125944361 12594436 2 SS ABILIFY ARIPIPRAZOLE 1 Intramuscular U 0 400 MG QD
125944361 12594436 3 SS GEODON ZIPRASIDONE HYDROCHLORIDEIPRASIDONE MESYLATE 1 Unknown U 0
125944361 12594436 4 SS TOPIRAMATE. TOPIRAMATE 1 Unknown U 0
125944361 12594436 5 SS HYDROXYZINE HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125944361 12594436 Condition aggravated
125944361 12594436 Delusion
125944361 12594436 Hallucination, auditory
125944361 12594436 Insomnia
125944361 12594436 Paranoia

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

no results found

Therapies reported

no results found