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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205773 | 7743416 | F | 7205773-0 | 20100707 | 20101230 | 20101231 | EXP | CN-PFIZER INC-2010176159 | PFIZERINC | 18 | MON | F | Y | 20101231 | MD | CHINA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205773 | 1015450445 | PS | SULPERAZON | 2 | INTRAVENOUS DRIP | 0.5G, Q12H | 050551 | ||||
| 7205773 | 1015450446 | SS | RIBAVIRIN | 2 | INTRAVENOUS DRIP | 90 MG, UNK | |||||
| 7205773 | 1015450447 | SS | CEFOPERAZONE SODIUM | 1 | INTRAVENOUS DRIP | 0.5G, Q12H |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7205773 | 1015450445 | INFECTION |
| 7205773 | 1015450446 | INFECTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7205773 | DE |
| 7205773 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7205773 | BLOOD PRESSURE DECREASED |
| 7205773 | BRONCHITIS |
| 7205773 | CYANOSIS |
| 7205773 | HEPATIC CONGESTION |
| 7205773 | HYPERSENSITIVITY |
| 7205773 | INTESTINAL CONGESTION |
| 7205773 | PULMONARY CONGESTION |
| 7205773 | SPLEEN CONGESTION |
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 |
|---|---|---|---|---|---|
| 7205773 | 1015450445 | 20100706 | 20100707 | 2 | DAY |
| 7205773 | 1015450446 | 20100701 | 20100706 | ||
| 7205773 | 1015450447 | 20100705 | 20100705 | 1 | DAY |