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
125285052 12528505 2 F 20160107 20160707 20160705 20160712 EXP GB-MHRA-EYC 00141486 GB-PFIZER INC-2016324206 PFIZER 16.00 YR F Y 62.51000 KG 20160712 CN GB GB

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
125285052 12528505 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 150-375, UNK 20699
125285052 12528505 2 C DESONIDE. DESONIDE 1 UNK 0
125285052 12528505 3 C FEXOFENADINE HYDROCHLORIDE. FEXOFENADINE HYDROCHLORIDE 1 UNK 0
125285052 12528505 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125285052 12528505 1 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125285052 12528505 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125285052 12528505 Asthenia
125285052 12528505 Dizziness
125285052 12528505 Dry eye
125285052 12528505 Dry mouth
125285052 12528505 Fatigue
125285052 12528505 Hot flush
125285052 12528505 Hypersomnia
125285052 12528505 Muscular weakness
125285052 12528505 Night sweats
125285052 12528505 Thirst

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
125285052 12528505 1 20160105 0