The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5903986 6775702 I 5903986-9 20080820 20080925 20080930 EXP FR-MERCK-0809FRA00089 MERCK HUMAN HEALTH DIVISION 75 YR F Y 20081001 OT FRANCE

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5903986 1010522452 PS PRIMAXIN 1 INTRAVENOUS 50587
5903986 1010522453 SS TEICOPLANIN 2 INTRAVENOUS
5903986 1010522454 SS AMIKACIN SULFATE 2 INTRAVENOUS DRIP
5903986 1010522455 C CIPROFLOXACIN 2 UNKNOWN
5903986 1010522456 SS FLUCONAZOLE 2 INTRAVENOUS
5903986 1010522457 C INSULIN 2 SUBCUTANEOUS
5903986 1010522458 C HEPARIN 2 UNKNOWN
5903986 1010522459 C ACEBUTOLOL 2 ORAL
5903986 1010522460 C BROMAZEPAM 2 ORAL
5903986 1010522461 C PRAVASTATIN SODIUM 2 ORAL
5903986 1010522462 C PHLOROGLUCINOL AND TRIMETHYLPHLOROGLUCINOL 2 ORAL
5903986 1010522463 C TRIMEBUTINE 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5903986 1010522452 SEPTIC SHOCK
5903986 1010522453 SEPTIC SHOCK
5903986 1010522454 SEPTIC SHOCK
5903986 1010522455 SEPTIC SHOCK
5903986 1010522456 SEPTIC SHOCK
5903986 1010522457 DIABETES MELLITUS
5903986 1010522458 THROMBOSIS PROPHYLAXIS
5903986 1010522460 ANXIETY
5903986 1010522461 DYSLIPIDAEMIA
5903986 1010522462 ABDOMINAL PAIN

Outcome of event

Event ID OUTC COD
5903986 HO

Reactions reported

Event ID PT
5903986 RASH MORBILLIFORM

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5903986 1010522452 20080813 20080823 11 DAY
5903986 1010522453 20080813 20080823 11 DAY
5903986 1010522454 20080813 20080818 6 DAY
5903986 1010522455 20080818 20080823 6 DAY
5903986 1010522456 20080813 20080823 11 DAY