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
127113081 12711308 1 I 20160825 20160902 20160902 EXP GB-MHRA-EYC 00144067 GB-DRREDDYS-GER/UKI/16/0082798 DR REDDYS 17.00 YR M Y 0.00000 20160902 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
127113081 12711308 1 PS FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Y U UNKNOWN 75465

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127113081 12711308 1 Depression

Outcome of event

Event ID CASEID OUTC COD
127113081 12711308 DS
127113081 12711308 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127113081 12711308 Abnormal weight gain
127113081 12711308 Anxiety
127113081 12711308 Deafness
127113081 12711308 Photophobia
127113081 12711308 Pruritus generalised
127113081 12711308 Suicidal ideation

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found