The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126533731 12653373 1 I 2013 20160610 20160815 20160815 EXP US-ABBVIE-16P-163-1649819-00 ABBVIE 45.79 YR F Y 93.07000 KG 20160815 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
126533731 12653373 1 PS VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral U UNKNOWN 88058
126533731 12653373 2 SS LYRICA PREGABALIN 1 Oral M11079 0 150 MG TID
126533731 12653373 3 SS LYRICA PREGABALIN 1 M11079 0
126533731 12653373 4 SS LYRICA PREGABALIN 1 M11079 0
126533731 12653373 5 SS GABAPENTIN. GABAPENTIN 1 Unknown U UNKNOWN 0
126533731 12653373 6 SS FENTANYL. FENTANYL 1 Unknown U 0
126533731 12653373 7 SS OXYCODONE OXYCODONE 1 Unknown U UNKNOWN 0
126533731 12653373 8 C MEDROL METHYLPREDNISOLONE 1 Oral 0 4 MG QID
126533731 12653373 9 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 0 75 MG BID
126533731 12653373 10 C XANAX ALPRAZOLAM 1 Oral 0 .5 MG TID
126533731 12653373 11 C DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Unknown PUMP 0
126533731 12653373 12 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
126533731 12653373 13 C PROAIR HFA ALBUTEROL SULFATE 1 0
126533731 12653373 14 C FLAVOXATE FLAVOXATE 1 Oral 0 100 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126533731 12653373 1 Product used for unknown indication
126533731 12653373 2 Fibromyalgia
126533731 12653373 3 Pain
126533731 12653373 4 Systemic lupus erythematosus
126533731 12653373 5 Product used for unknown indication
126533731 12653373 6 Product used for unknown indication
126533731 12653373 7 Product used for unknown indication
126533731 12653373 8 Systemic lupus erythematosus
126533731 12653373 9 Depression
126533731 12653373 10 Depression
126533731 12653373 11 Pain
126533731 12653373 12 Asthma
126533731 12653373 13 Asthma
126533731 12653373 14 Bladder spasm

Outcome of event

Event ID CASEID OUTC COD
126533731 12653373 OT
126533731 12653373 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126533731 12653373 Abnormal dreams
126533731 12653373 Activities of daily living impaired
126533731 12653373 Bone pain
126533731 12653373 Diarrhoea
126533731 12653373 Dizziness
126533731 12653373 Drug dose omission
126533731 12653373 Hypophagia
126533731 12653373 Malaise
126533731 12653373 Mobility decreased
126533731 12653373 Nausea
126533731 12653373 Oxygen saturation decreased
126533731 12653373 Photophobia
126533731 12653373 Pneumonia
126533731 12653373 Septic shock
126533731 12653373 Somnolence
126533731 12653373 Weight decreased
126533731 12653373 Weight increased
126533731 12653373 Withdrawal syndrome

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126533731 12653373 2 2013 0
126533731 12653373 11 201310 0
126533731 12653373 12 2015 0
126533731 12653373 14 2012 0