The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
4871961 5959647 I 4871961-1 20051216 20051221 20051230 EXP S05-USA-05277-01 FOREST LABORATORIES INC. 79 YR F N 20051228 CN 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
4871961 1006786239 PS NAMENDA 1 ORAL 5 MG QD PO Y D 21487
4871961 1006814227 C FLONASE (FLUTICASONE PROPINATE) 2
4871961 1006814228 C AMBIEN 1
4871961 1006814229 C PREVACID 1
4871961 1006814230 C HYOSCYAMINE 2
4871961 1006814231 C PRAVACHOL 1
4871961 1006814232 C ACETAMINOPHEN 1
4871961 1006814233 C COZAAR 1
4871961 1006814234 C VICODIN 1
4871961 1006814235 C DIFLUCAN (FLUCONAZOLE) 2
4871961 1006814236 C LORAZEPAM 1
4871961 1006814237 C LIDOCAINE 1
4871961 1006814238 C DITROPAN 1
4871961 1006814239 C ELMIRON 1
4871961 1006814240 C URISPAS 1
4871961 1006814241 C PREMARIN 1
4871961 1006814242 C NYSTATIN 1
4871961 1006814243 C METOPROLOL 2
4871961 1006814244 C DARVOCET (PROPOXYPHENE/ACETAMINOPHEN) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4871961 1006786239 CEREBROVASCULAR ACCIDENT
4871961 1006786239 NERVOUS SYSTEM DISORDER

Outcome of event

Event ID OUTC COD
4871961 OT

Reactions reported

Event ID PT
4871961 DEAFNESS UNILATERAL
4871961 HYPOACUSIS

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4871961 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4871961 1006786239 20051212 20051220