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
123207393 12320739 3 F 201603 20160909 20160429 20160912 EXP CA-HLSUS-2016-CA-000065 HLS THERAPEUTICS 65.00 YR E F Y 50.00000 KG 20160912 MD CA CA

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
123207393 12320739 1 PS CLOZARIL CLOZAPINE 1 Oral 100 MG DAILY 0 100 MG TABLET
123207393 12320739 2 C RISPERDAL RISPERIDONE 1 Oral 1 MG AT SUPPER AND 2 MG HS 0 BID
123207393 12320739 3 C EPIVAL DIVALPROEX SODIUM 1 Oral 500 MG BID AND 750 MG HS 0 BID
123207393 12320739 4 C Atropine 1% ATROPINE 1 Sublingual 1-2 DROPS BID 0 BID
123207393 12320739 5 C KEMADRIN PROCYCLIDINE HYDROCHLORIDE 1 Oral 5 MG BID 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123207393 12320739 1 Schizoaffective disorder bipolar type
123207393 12320739 2 Schizoaffective disorder bipolar type
123207393 12320739 3 Schizoaffective disorder bipolar type
123207393 12320739 4 Schizoaffective disorder bipolar type
123207393 12320739 5 Schizoaffective disorder bipolar type

Outcome of event

Event ID CASEID OUTC COD
123207393 12320739 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
123207393 12320739 Asthenia
123207393 12320739 Blood creatinine increased
123207393 12320739 Choking
123207393 12320739 Dysphagia
123207393 12320739 Haemoglobin decreased
123207393 12320739 Impaired self-care

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
123207393 12320739 1 20010322 20160424 0