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
5374686 6005796 I 5374686-1 20060309 20070619 20070629 EXP US-JNJFOC-20060302705 JOHNSON + JOHNSON PHARMACEUTICAL R+D F Y 62.6 KG 20070629 MD 20060321 UNITED STATES

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
5374686 1008646770 PS YONDELIS 2 INTRAVENOUS 50286
5374686 1008646771 SS DOXIL 1 INTRAVENOUS 050718
5374686 1008646772 C PROTONIX 1
5374686 1008646773 C AMBIEN 1
5374686 1008646774 C MARINOL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5374686 1008646770 OVARIAN CANCER
5374686 1008646771 OVARIAN CANCER

Outcome of event

Event ID OUTC COD
5374686 DE
5374686 HO
5374686 LT

Reactions reported

Event ID PT
5374686 ARTERIAL THROMBOSIS LIMB
5374686 CARDIAC ARREST
5374686 DEHYDRATION
5374686 ELECTROMECHANICAL DISSOCIATION
5374686 HYPOXIA
5374686 PANCYTOPENIA
5374686 PERIPHERAL ISCHAEMIA
5374686 RENAL FAILURE ACUTE
5374686 RESPIRATORY FAILURE
5374686 SEPSIS
5374686 URINARY TRACT INFECTION

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

no results found

Therapies reported

no results found