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
124336942 12433694 2 F 2015 20160623 20160603 20160705 PER US-JNJFOC-20160513829 JANSSEN 0.00 A M Y 88.45000 KG 20160705 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
124336942 12433694 1 PS INVEGA SUSTENNA PALIPERIDONE PALMITATE 1 Intramuscular N UNKNOWN;UNKNOWN;UNKNOWN 22264 234 MG INJECTION /month
124336942 12433694 2 SS INVEGA PALIPERIDONE 1 Oral N UNKNOWN 21999 6 MG OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET QD
124336942 12433694 3 C TYLENOL ACETAMINOPHEN 1 Unknown 325 MG AND 30MG 0 325 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124336942 12433694 1 Schizophrenia
124336942 12433694 2 Schizophrenia
124336942 12433694 3 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124336942 12433694 Drug level increased
124336942 12433694 Injection site rash
124336942 12433694 Limb discomfort
124336942 12433694 Memory impairment
124336942 12433694 Visual acuity reduced
124336942 12433694 Weight increased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124336942 12433694 2 2015 0