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
125358512 12535851 2 F 20160624 20160707 20160707 EXP GB-MHRA-EYC 00141281 GB-WATSON-2016-14668 ACTAVIS 66.00 YR F Y 0.00000 20160707 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
125358512 12535851 1 SS Clarithromycin (Unknown) CLARITHROMYCIN 1 Oral UNK UNK, UNKNOWN Y UNCONFIRMED 0 UNK
125358512 12535851 2 PS Lansoprazole (Unknown) LANSOPRAZOLE 1 Oral UNK UNK, UNKNOWN Y UNCONFIRMED 203306 UNK
125358512 12535851 3 SS AMOXICILLIN. AMOXICILLIN 1 Oral UNK UNK, UNKNOWN Y UNCONFIRMED 0 UNK

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125358512 12535851 1 Product used for unknown indication
125358512 12535851 2 Product used for unknown indication
125358512 12535851 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125358512 12535851 OT
125358512 12535851 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125358512 12535851 Hypoglycaemia

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
125358512 12535851 1 20160528 20160531 0
125358512 12535851 2 20160528 20160531 0
125358512 12535851 3 20160528 20160531 0