The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8624259 8742049 F 8624259-X 20120811 20120817 20120827 EXP US-JNJFOC-20120807500 JANSSEN PHARMACEUTICALS, INC. 42 YR M Y 125 KG 20120827 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8624259 1020672929 SS PALIPERIDONE PALMITATE 2 INTRAMUSCULAR 365791;365790
8624259 1020672935 C TRAZODONE HYDROCHLORIDE 1 ORAL
8624259 1020672932 SS PALIPERIDONE PALMITATE 2 INTRAMUSCULAR 022264
8624259 1020672931 SS PALIPERIDONE PALMITATE 2 INTRAMUSCULAR 076952
8624259 1020672934 C CITALOPRAM HYDROBROMIDE 1 ORAL
8624259 1020672936 C PALIPERDONE 2 ORAL
8624259 1020672930 PS PALIPERIDONE PALMITATE 2 INTRAMUSCULAR 365791;365790 022264
8624259 1020672933 C RISPERIDONE 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
8624259 1020672929 SCHIZOPHRENIA
8624259 1020672935 DEPRESSION
8624259 1020672934 DEPRESSION
8624259 1020672936 PRODUCT USED FOR UNKNOWN INDICATION
8624259 1020672933 SCHIZOPHRENIA

Outcome of event

Event ID OUTC COD
8624259 HO

Reactions reported

Event ID PT
8624259 SUICIDAL IDEATION
8624259 NAUSEA
8624259 VOMITING

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8624259 1020672929 20120802 20120802
8624259 1020672935 20120325
8624259 1020672934 20120325
8624259 1020672936 20120720 20120725
8624259 1020672930 20120808 20120808
8624259 1020672933 20120325 20120719