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
7117602 7567246 F 7117602-4 20100802 20101112 20101122 EXP JP-AMGEN-KDC434533 AMGENSAFETY YR Y 20101122 OT 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
7117602 1015168226 PS PANITUMUMAB 2 INTRAVENOUS DRIP 6 MG/KG, Q2WK
7117602 1015168227 C POLARAMINE 1 INTRAVENOUS DRIP
7117602 1015168228 C ANTIHISTAMINES 2 UNKNOWN UNK UNK, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7117602 1015168226 COLORECTAL CANCER
7117602 1015168227 ALLERGY PROPHYLAXIS
7117602 1015168228 PROPHYLAXIS

Outcome of event

Event ID OUTC COD
7117602 HO
7117602 OT

Reactions reported

Event ID PT
7117602 COLON CANCER METASTATIC
7117602 DERMATITIS ACNEIFORM
7117602 HENOCH-SCHONLEIN PURPURA
7117602 HYDRONEPHROSIS
7117602 HYPOALBUMINAEMIA
7117602 LEUKOCYTOCLASTIC VASCULITIS
7117602 MALIGNANT NEOPLASM PROGRESSION
7117602 METASTASES TO PERITONEUM
7117602 PLATELET COUNT DECREASED
7117602 PROTEIN TOTAL DECREASED
7117602 PROTEINURIA
7117602 RENAL FAILURE ACUTE
7117602 SCAB
7117602 URETERIC OBSTRUCTION
7117602 WHITE BLOOD CELL COUNT INCREASED

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
7117602 1015168226 20100720 20100802 14 DAY
7117602 1015168227 20100720