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
125695521 12569552 1 I 20160707 20160719 20160719 EXP US-MLMSERVICE-20160629-0303882-1 US-ALKEM LABORATORIES LIMITED-US-ALKEM-2016-00062 ALKEM 25.00 YR F Y 0.00000 20160718 MD US US

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
125695521 12569552 1 PS GABAPENTIN. GABAPENTIN 1 UNKNOWN 90858
125695521 12569552 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNKNOWN 0
125695521 12569552 3 SS NICOTINE. NICOTINE 1 UNKNOWN 0
125695521 12569552 4 SS CLONAZEPAM. CLONAZEPAM 1 Oral UNKNOWN 0
125695521 12569552 5 SS DIAMORPHINE DIACETYLMORPHINE 1 Oral UNKNOWN 0
125695521 12569552 6 SS TRAZODONE TRAZODONE HYDROCHLORIDE 1 UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125695521 12569552 1 Product used for unknown indication
125695521 12569552 2 Product used for unknown indication
125695521 12569552 3 Product used for unknown indication
125695521 12569552 4 Product used for unknown indication
125695521 12569552 5 Product used for unknown indication
125695521 12569552 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125695521 12569552 LT
125695521 12569552 OT
125695521 12569552 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125695521 12569552 Hypoglycaemia
125695521 12569552 Hypotension
125695521 12569552 Myocardial stunning
125695521 12569552 Overdose
125695521 12569552 Respiratory failure

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

no results found

Therapies reported

no results found