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 |