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
6698964 7367825 F 6698964-9 20100420 20100427 EXP B0643299A GLAXOSMITHKLINE 18 YR F Y 20100427 MD JAPAN

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
6698964 1013578723 SS ATARAX 1 INTRAVENOUS 25MG THREE TIMES PER DAY
6698964 1013578724 PS ZOVIRAX 1 ORAL 200MG PER DAY 018603
6698964 1013578725 SS SANDIMMUNE 1 INTRAVENOUS 120MG PER DAY
6698964 1013578726 SS MEROPEN 2 INTRAVENOUS 2G TWICE PER DAY
6698964 1013578727 SS AMPHOTERICIN B 1 INTRAVENOUS 50MG PER DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6698964 1013578723 PAIN
6698964 1013578724 ANTIVIRAL PROPHYLAXIS
6698964 1013578725 GRAFT VERSUS HOST DISEASE
6698964 1013578726 INFECTION
6698964 1013578727 INFECTION

Outcome of event

Event ID OUTC COD
6698964 HO
6698964 OT

Reactions reported

Event ID PT
6698964 PERSONALITY CHANGE

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
6698964 1013578723 20091215 20100311 87 DAY
6698964 1013578724 20100126
6698964 1013578725 20091221 20100123 34 DAY
6698964 1013578726 20091221 20100224 66 DAY
6698964 1013578727 20091128 20100305 98 DAY