Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124877182 | 12487718 | 2 | F | 20160704 | 20160622 | 20160716 | EXP | US-AUROBINDO-AUR-APL-2016-08074 | AUROBINDO | 24.00 | YR | F | Y | 0.00000 | 20160716 | OT | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124877182 | 12487718 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | UNK | U | U | 70734 | ||||||||
124877182 | 12487718 | 2 | SS | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | Unknown | UNK | U | U | 0 | ||||||||
124877182 | 12487718 | 3 | SS | COPPER | COPPER | 1 | Intra-uterine | UNK | U | U | 0 | ||||||||
124877182 | 12487718 | 4 | SS | FENTANYL. | FENTANYL | 1 | Intravenous (not otherwise specified) | 100 ?G, UNK | U | U | 0 | 100 | UG | ||||||
124877182 | 12487718 | 5 | SS | MIDAZOLAM | MIDAZOLAMMIDAZOLAM HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 2 MG, UNK | U | U | 0 | 2 | MG | ||||||
124877182 | 12487718 | 6 | SS | RHOGAM | HUMAN RHO(D) IMMUNE GLOBULIN | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124877182 | 12487718 | 1 | Product used for unknown indication |
124877182 | 12487718 | 2 | Product used for unknown indication |
124877182 | 12487718 | 3 | Product used for unknown indication |
124877182 | 12487718 | 4 | Anaesthesia |
124877182 | 12487718 | 5 | Anaesthesia |
124877182 | 12487718 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124877182 | 12487718 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124877182 | 12487718 | Anaphylactic reaction | |
124877182 | 12487718 | Chest pain | |
124877182 | 12487718 | Dyspnoea | |
124877182 | 12487718 | Kounis syndrome | |
124877182 | 12487718 | Lactic acidosis | |
124877182 | 12487718 | Swelling face | |
124877182 | 12487718 | Urticaria |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |