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
5117569 4192499 F 5117569-4 20030303 20040812 20060929 EXP 200416123US AVENTIS PHARMACEUTICALS, INC. F Y 74.54 KG 20060929 MD 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
5117569 1007716858 PS LOVENOX 1 SUBCUTANEOUS UNK 20164
5117569 1007716859 SS LOVENOX 1 SUBCUTANEOUS UNK 020164
5117569 1007716860 SS LOVENOX 1 SUBCUTANEOUS UNK 020164
5117569 1007716861 SS LOVENOX 1 SUBCUTANEOUS UNK 020164
5117569 1007716862 C NUBAIN 1 INTRAVENOUS UNK
5117569 1007716863 C PITOCIN 1 INTRAVENOUS DOSE: 20/1000CC LR UNK
5117569 1007716864 C PERCOCET 1 DOSE: 2 TABLETS UNK
5117569 1007716865 C XANAX 1
5117569 1007716866 C DEMEROL 1
5117569 1007716867 C DILAUDID 1 INTRAVENOUS FREQUENCY: EVERY 6 TO 8 HOURS UNK
5117569 1007716868 C ATIVAN 1 INTRAVENOUS
5117569 1007716869 C PHENERGAN 1 INTRAMUSCULAR
5117569 1007716870 C TYLENOL 1 ORAL
5117569 1007716871 C VITAMINS 2 DOSE: UNK
5117569 1007716872 C COUMADIN 1 DOSE: UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117569 1007716858 DEEP VEIN THROMBOSIS

Outcome of event

Event ID OUTC COD
5117569 OT

Reactions reported

Event ID PT
5117569 ARTHRALGIA
5117569 BLOOD ALBUMIN DECREASED
5117569 BLOOD ALKALINE PHOSPHATASE INCREASED
5117569 CHORIOAMNIONITIS
5117569 DRUG EXPOSURE DURING PREGNANCY
5117569 HAEMATOCRIT DECREASED
5117569 HAEMOGLOBIN DECREASED
5117569 MUSCULOSKELETAL CHEST PAIN
5117569 PHLEBITIS
5117569 PLACENTAL INFARCTION
5117569 PLACENTAL INSUFFICIENCY
5117569 PLATELET COUNT INCREASED
5117569 RED BLOOD CELL MORPHOLOGY ABNORMAL
5117569 UMBILICAL CORD ABNORMALITY
5117569 VASCULITIS
5117569 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
5117569 1007716858 20030201
5117569 1007716859 20030701
5117569 1007716860 20030728 20030728
5117569 1007716861 20060728
5117569 1007716862 20030727 20030727
5117569 1007716863 20030727 20030727
5117569 1007716864 20030727
5117569 1007716866 20030728
5117569 1007716867 20030728 20030728
5117569 1007716869 20030728
5117569 1007716870 20030727
5117569 1007716872 20020701 20021001