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
125482261 12548226 1 I 20140107 0 20160711 20160711 DIR 49.00 YR N 168.00000 LBS 20160710 N 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
125482261 12548226 1 PS VENLAFAXINE HCL ER 37.5 PFIZER VENLAFAXINE HYDROCHLORIDE 1 Oral N Y 0 HS
125482261 12548226 3 C ATENELOL ATENOLOL 1 0
125482261 12548226 5 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
125482261 12548226 7 C PROAIR HFA ALBUTEROL SULFATE 1 0
125482261 12548226 9 C CLOZEPAM 2 0
125482261 12548226 11 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 0
125482261 12548226 13 C VITAMIN B12 CYANOCOBALAMIN 1 0
125482261 12548226 15 C BABY ASPIRIN ASPIRIN 1 0
125482261 12548226 17 C TYLENOL ACETAMINOPHEN 1 0
125482261 12548226 19 C ADVIL IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125482261 12548226 1 Anxiety
125482261 12548226 1 Depression

Outcome of event

Event ID CASEID OUTC COD
125482261 12548226 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125482261 12548226 Constipation
125482261 12548226 Diarrhoea
125482261 12548226 Dizziness
125482261 12548226 Gastric disorder
125482261 12548226 Myocardial infarction
125482261 12548226 Nausea
125482261 12548226 Suicidal ideation
125482261 12548226 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
125482261 12548226 1 3 YR