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
126376501 12637650 1 I 20160621 20160809 20160809 PER US-ABBVIE-16P-163-1658963-00 ABBVIE 0.00 M Y 0.00000 20160809 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
126376501 12637650 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown U UNKNOWN 18723 TABLET
126376501 12637650 2 SS LITHIUM. LITHIUM 1 Unknown U UNKNOWN 0
126376501 12637650 3 SS RISPERDAL RISPERIDONE 1 Unknown U UNKNOWN 0
126376501 12637650 4 SS HALDOL HALOPERIDOL 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126376501 12637650 1 Product used for unknown indication
126376501 12637650 2 Product used for unknown indication
126376501 12637650 3 Product used for unknown indication
126376501 12637650 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126376501 12637650 Drug ineffective
126376501 12637650 Skin discolouration
126376501 12637650 Weight increased

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

no results found

Therapies reported

no results found