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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126839752 | 12683975 | 2 | F | 20160913 | 20160825 | 20160919 | EXP | US-PFIZER INC-2016398331 | PFIZER | 78.00 | YR | F | Y | 0.00000 | 20160919 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126839752 | 12683975 | 1 | PS | AROMASIN | EXEMESTANE | 1 | 25 MG, 1X/DAY (1 AM) | 20753 | 25 | MG | COATED TABLET | QD | |||||||
126839752 | 12683975 | 2 | C | DICYCLOMINE | DICYCLOMINE HYDROCHLORIDE | 1 | 10 MG, TWICE A DAY (10 MG 1 AM +1 PM) | 0 | 10 | MG | BID | ||||||||
126839752 | 12683975 | 3 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | 0.5 MG, 2X/DAY (1 AM + 1 PM) | 0 | .5 | MG | BID | ||||||||
126839752 | 12683975 | 4 | C | PROMETHAZINE | PROMETHAZINEPROMETHAZINE HYDROCHLORIDE | 1 | 2.5 MG, AS NEEDED | 0 | 2.5 | MG | |||||||||
126839752 | 12683975 | 5 | C | ASPIRIN. | ASPIRIN | 1 | UNK, 1X/DAY (AM EVERY DAY) | 0 | QD | ||||||||||
126839752 | 12683975 | 6 | C | TYLENOL | ACETAMINOPHEN | 1 | 650 MG, TWICE A DAY AS NEEDED (2 AM-2 PM) | 0 | 650 | MG | |||||||||
126839752 | 12683975 | 7 | C | FAMOTIDINE. | FAMOTIDINE | 1 | 20 MG, AS NEEDED (1 OR 2) | 0 | 20 | MG | |||||||||
126839752 | 12683975 | 8 | C | AMOXICILLIN. | AMOXICILLIN | 1 | UNK UNK, AS NEEDED (500 EVERY 8 HOURS) | 0 | |||||||||||
126839752 | 12683975 | 9 | C | PRUNE | PRUNE | 1 | 16 OZ EVERY AM AS NEEDED | 0 | |||||||||||
126839752 | 12683975 | 10 | C | CORRECTOL NOS | BISACODYL OR DOCUSATE SODIUM | 1 | 5 MG, 1X/DAY (PM) | 0 | 5 | MG | QD | ||||||||
126839752 | 12683975 | 11 | C | CITRATE | CITRIC ACID MONOHYDRATE | 1 | 1400 MG (EVERY PM) | 0 | 1400 | MG | QD | ||||||||
126839752 | 12683975 | 12 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | EVERY PM | 0 | QD | ||||||||||
126839752 | 12683975 | 13 | C | CHLOR | 2 | 4 MG, EVERY 4 HOURS | 0 | 4 | MG | TABLET | |||||||||
126839752 | 12683975 | 14 | C | STOOL SOFTENER | DOCUSATE CALCIUM | 1 | 2 DF, UNK | 0 | 2 | DF | |||||||||
126839752 | 12683975 | 15 | C | LOVASTATIN. | LOVASTATIN | 1 | 20 MG, 1X/DAY (PM) | 0 | 20 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126839752 | 12683975 | 3 | Nervous system disorder |
126839752 | 12683975 | 4 | Nausea |
126839752 | 12683975 | 6 | Pain |
126839752 | 12683975 | 7 | Acidosis |
126839752 | 12683975 | 8 | Kidney infection |
126839752 | 12683975 | 9 | Laxative supportive care |
126839752 | 12683975 | 10 | Laxative supportive care |
126839752 | 12683975 | 13 | Hypersensitivity |
126839752 | 12683975 | 14 | Laxative supportive care |
126839752 | 12683975 | 15 | Blood cholesterol abnormal |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126839752 | 12683975 | OT |
126839752 | 12683975 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126839752 | 12683975 | Facial paralysis | |
126839752 | 12683975 | Fall | |
126839752 | 12683975 | Head injury | |
126839752 | 12683975 | Hypertension | |
126839752 | 12683975 | Loss of consciousness |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |