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
127225381 12722538 1 I 20150401 20160902 20160907 20160907 EXP GB-MHRA-EYC 00144434 GB-PFIZER INC-2016416410 PFIZER 64.00 YR M Y 88.00000 KG 20160907 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
127225381 12722538 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, UNK Y SEVERAL 20699 150 MG
127225381 12722538 2 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
127225381 12722538 3 C LIPITOR ATORVASTATIN CALCIUM 1 UNK 0
127225381 12722538 4 C OMEPRAZOLE. OMEPRAZOLE 1 UNK 0
127225381 12722538 5 C RAMIPRIL. RAMIPRIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127225381 12722538 1 Antidepressant therapy

Outcome of event

Event ID CASEID OUTC COD
127225381 12722538 DS
127225381 12722538 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127225381 12722538 Acrophobia
127225381 12722538 Asthenia
127225381 12722538 Diarrhoea
127225381 12722538 Dizziness
127225381 12722538 Drug ineffective
127225381 12722538 Drug withdrawal headache
127225381 12722538 Influenza like illness
127225381 12722538 Insomnia
127225381 12722538 Myalgia
127225381 12722538 Nightmare
127225381 12722538 Product substitution issue
127225381 12722538 Psychiatric symptom
127225381 12722538 Tinnitus
127225381 12722538 Withdrawal syndrome

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
127225381 12722538 1 20110101 20150605 0