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
4719243 6011174 I 4719243-2 20050708 20050719 EXP USA-2005-0020743 PURDUE PHARMA L.P. 30 YR F N 22.7 KG 20050718 MD BELGIUM

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
4719243 1006226797 PS MORPHINE SULFATE 1 Y D 19516
4719243 1006264532 SS POSACONAZOLE 1 ORAL 20 ML, DAILY, ORAL; SEE IMAGE Y D 80559-107

Indications of drugs used

Event ID DRUG SEQ INDI PT
4719243 1006226797 PAIN
4719243 1006264532 FUNGAL INFECTION

Outcome of event

Event ID OUTC COD
4719243 OT
4719243 RI

Reactions reported

Event ID PT
4719243 ALANINE AMINOTRANSFERASE INCREASED
4719243 ASPARTATE AMINOTRANSFERASE INCREASED
4719243 BACTERIA SPUTUM IDENTIFIED
4719243 BACTERIAL INFECTION
4719243 BILIRUBIN CONJUGATED INCREASED
4719243 BLOOD ALBUMIN DECREASED
4719243 BLOOD ALKALINE PHOSPHATASE INCREASED
4719243 BLOOD BILIRUBIN INCREASED
4719243 BLOOD FIBRINOGEN DECREASED
4719243 BLOOD UREA INCREASED
4719243 C-REACTIVE PROTEIN INCREASED
4719243 FIBRIN D DIMER INCREASED
4719243 GAMMA-GLUTAMYLTRANSFERASE INCREASED
4719243 HAEMATOCRIT DECREASED
4719243 HYPERCAPNIA
4719243 LUNG DISORDER
4719243 LUNG INFILTRATION
4719243 LYMPHOCYTE COUNT INCREASED
4719243 LYMPHOCYTE PERCENTAGE DECREASED
4719243 MICROSPORUM INFECTION
4719243 MONOCYTE COUNT INCREASED
4719243 MONOCYTE PERCENTAGE INCREASED
4719243 NEUTROPHIL PERCENTAGE DECREASED
4719243 NODULE
4719243 PLATELET COUNT DECREASED
4719243 PLEURITIC PAIN
4719243 PNEUMONIA
4719243 PROTEIN TOTAL DECREASED
4719243 RED BLOOD CELL COUNT DECREASED
4719243 RED CELL DISTRIBUTION WIDTH INCREASED
4719243 RESPIRATORY FAILURE
4719243 RETICULOCYTE COUNT DECREASED
4719243 WHITE BLOOD CELL COUNT DECREASED
4719243 ZYGOMYCOSIS

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

Event ID RPSR COD
4719243 FGN
4719243 HP
4719243 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4719243 1006226797 20050518
4719243 1006264532 20050426 20050519
4719243 1006264532 20050519
4719243 1006264532 20050426