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
6544681 7579885 F #1 6544681-5 20091209 20100105 20100115 EXP AMAG200900076 AMAG PHARMACEUTICALS, INC. 68 YR F N 54.5 KG 20100114 OT 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
6544681 1012974154 PS FERAHEME 1 INTRAVENOUS 510 MG, SINGLE, INTRAVENOUS D D 09060402 20110630 22180
6544681 1013011783 SS EPINEPHRINE 1 INTRAVENOUS 1 MG, SINGLE, INTRAVENOUS D D
6544681 1013011784 SS SOLU-MEDROL 1 INTRAVENOUS 140 MG, SINGLE, INTRAVENOUS D D
6544681 1013011785 C ADVAIR DISKUS 100/50 1 22180
6544681 1013011786 C DIGOXIN 1 22180
6544681 1013011787 C FOLIC ACID 1 22180
6544681 1013011788 C SPIRIVA 1 22180
6544681 1013011789 C VASOTEC 1 22180
6544681 1013011790 C ASPIRIN 1 22180
6544681 1013011791 C EPOGEN 1 22180
6544681 1013011792 C HEPARIN 1 22180
6544681 1013011793 C LANTUS 1 22180
6544681 1013011794 C METOPROLOL TARTRATE 1 22180
6544681 1013011795 C NEURONTIN 1 22180
6544681 1013011796 C ZEMPLAR 1 22180
6544681 1013011797 C RENAGEL 1 22180
6544681 1013011798 C VANCOMYCIN 1 22180

Indications of drugs used

Event ID DRUG SEQ INDI PT
6544681 1012974154 IRON DEFICIENCY ANAEMIA

Outcome of event

Event ID OUTC COD
6544681 HO

Reactions reported

Event ID PT
6544681 BLOOD PRESSURE INADEQUATELY CONTROLLED
6544681 CONDITION AGGRAVATED
6544681 DYSPNOEA
6544681 LIP SWELLING
6544681 NAUSEA
6544681 SWOLLEN TONGUE
6544681 TACHYCARDIA

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

Event ID RPSR COD
6544681 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6544681 1012974154 20091209 20091209
6544681 1013011783 20091209 20091209
6544681 1013011784 20091209 20091209