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
127911871 12791187 1 I 0 20160928 20160928 DIR US-FDA-351749 FDA-CTU 67.00 YR M N 77.85000 KG 20160928 N 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
127911871 12791187 1 PS PAROXETINE HCL PAROXETINE HYDROCHLORIDE 1 Oral ? QUANTITY:1 TABLET(S);? 20170711 99 1 DF COATED TABLET QD
127911871 12791187 3 C SIMVASTATIN. SIMVASTATIN 1 0
127911871 12791187 5 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 0
127911871 12791187 7 C LORAZEPAM. LORAZEPAM 1 0
127911871 12791187 9 C PROBIOTICS PROBIOTICS NOS 1 0
127911871 12791187 11 C MELATONIN MELATONIN 1 0
127911871 12791187 13 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127911871 12791187 1 Anxiety
127911871 12791187 1 Depression
127911871 12791187 1 Panic attack

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127911871 12791187 Hyperhidrosis
127911871 12791187 Somnolence

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
127911871 12791187 1 20160711 0