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
127425041 12742504 1 I 20150401 20160902 20160914 20160914 EXP GB-MHRA-EYC 00144434 GB-TEVA-690897ACC TEVA 64.00 YR M Y 88.00000 KG 20160914 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
127425041 12742504 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral Y U SEVERAL 76690 150 MG
127425041 12742504 2 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
127425041 12742504 3 C LIPITOR ATORVASTATIN CALCIUM 1 0
127425041 12742504 4 C OMEPRAZOLE. OMEPRAZOLE 1 0
127425041 12742504 5 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127425041 12742504 1 Antidepressant therapy

Outcome of event

Event ID CASEID OUTC COD
127425041 12742504 OT
127425041 12742504 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127425041 12742504 Acrophobia
127425041 12742504 Asthenia
127425041 12742504 Diarrhoea
127425041 12742504 Dizziness
127425041 12742504 Drug ineffective
127425041 12742504 Drug withdrawal headache
127425041 12742504 Influenza like illness
127425041 12742504 Insomnia
127425041 12742504 Myalgia
127425041 12742504 Nightmare
127425041 12742504 Product substitution issue
127425041 12742504 Psychiatric symptom
127425041 12742504 Tinnitus
127425041 12742504 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
127425041 12742504 1 20110101 20150605 0