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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92800215 | 9280021 | 5 | F | 20160704 | 20130509 | 20160718 | EXP | US-RANBAXY-2013US-68648 | RANBAXY | 53.00 | YR | M | Y | 0.00000 | 20160718 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92800215 | 9280021 | 1 | PS | Pantoprazole | PANTOPRAZOLE SODIUM | 1 | Oral | 40 MG, QD | Y | 200794 | 40 | MG | |||||||
92800215 | 9280021 | 2 | C | DILTIAZEM. | DILTIAZEM | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
92800215 | 9280021 | 3 | C | HEPARIN | HEPARIN SODIUM | 1 | Intravenous (not otherwise specified) | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
92800215 | 9280021 | 1 | Prophylaxis against gastrointestinal ulcer |
92800215 | 9280021 | 2 | Arrhythmia |
92800215 | 9280021 | 3 | Anticoagulant therapy |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
92800215 | 9280021 | LT |
92800215 | 9280021 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
92800215 | 9280021 | Hypomagnesaemia | |
92800215 | 9280021 | Torsade de pointes | |
92800215 | 9280021 | Unresponsive to stimuli | |
92800215 | 9280021 | Ventricular tachycardia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |