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
126649861 12664986 1 I 20160518 20160810 20160818 20160818 EXP AM20160930 FR-MYLANLABS-2016M1034532 MYLAN 0.00 Y 0.00000 20160818 OT FR FR

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
126649861 12664986 1 PS BISOCE 5 MG, COMPRIM? PELLICUL? S?CABLE BISOPROLOL 1 Oral 1 DF, UNK Y U 75831 1 DF TABLET
126649861 12664986 2 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 40 MG, UNK Y U 0 40 MG
126649861 12664986 3 SS FRAGMINE DALTEPARIN SODIUM 1 Subcutaneous 1 DF, UNK 0 1 DF SOLUTION FOR INJECTION
126649861 12664986 4 SS KEPPRA LEVETIRACETAM 1 Oral 500 MG, BID 11000 MG Y U 0 500 MG FILM-COATED TABLET BID
126649861 12664986 5 C DIFFU K POTASSIUM CHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126649861 12664986 1 Atrial fibrillation
126649861 12664986 2 Product used for unknown indication
126649861 12664986 3 Thrombosis prophylaxis
126649861 12664986 4 Status epilepticus
126649861 12664986 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126649861 12664986 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126649861 12664986 Metabolic encephalopathy

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
126649861 12664986 1 20160517 20160603 0
126649861 12664986 2 20160514 20160531 0
126649861 12664986 3 20160513 0
126649861 12664986 4 20160508 20160521 0