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
6733953 7394546 I 6733953-7 20100207 20100506 20100520 EXP DE-WYE-H15067710 WYETH PHARMACEUTICALS INC. 3 YR M Y 17.4 KG 20100520 OT GERMANY

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
6733953 1013721941 PS PANTOPRAZOLE SODIUM 1 INTRAVENOUS 020988
6733953 1013721942 C FORTUM 2 INTRAVENOUS
6733953 1013721943 C ALBUMIN (HUMAN) 1 INTRAVENOUS UNKNOWN
6733953 1013721944 C DIPYRONE TAB 1 ORAL UNKNOWN
6733953 1013721945 C FENISTIL 2 ORAL UNKNOWN
6733953 1013721946 C HEPARIN 1 INTRAVENOUS UNKNOWN
6733953 1013721947 C TOBRAMYCIN 1 INTRAVENOUS
6733953 1013721948 C CLONT 2 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6733953 1013721941 ABDOMINAL PAIN
6733953 1013721942 SYSTEMIC INFLAMMATORY RESPONSE SYNDROME
6733953 1013721947 SYSTEMIC INFLAMMATORY RESPONSE SYNDROME
6733953 1013721948 SYSTEMIC INFLAMMATORY RESPONSE SYNDROME

Outcome of event

Event ID OUTC COD
6733953 HO

Reactions reported

Event ID PT
6733953 HYPERTRIGLYCERIDAEMIA

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
6733953 1013721941 20100203 20100207 5 DAY
6733953 1013721942 20100203 20100211 9 DAY
6733953 1013721947 20100203 20100211 9 DAY
6733953 1013721948 20100203 20100209 7 DAY