SUMMARY PRODUCT INFORMATION 3 INDICATIONS AND CLINICAL USE 3 CONTRAINDICATIONS 3 WARNINGS AND PRECAUTIONS 4 ADVERSE REACTIONS 5 DRUG INTERACTIONS 14 DOSAGE AND ADMINISTRATION 14 OVERDOSAGE 16 ACTION AND CLINICAL PHARMACOLOGY 17 STORAGE AND STABILITY 18 DOSAGE FORMS, COMPOSITION AND PACKAGING 18

PART II: SCIENTIFIC INFORMATION 19

PART III: CONSUMER INFORMATION. 27

PART I: HEALTH PROFESSIONAL INFORMATION SUMMARY PRODUCT INFORMATION

CONTRAINDICATIONS

The use of VENOFER (Iron Sucrose Injection, USP) is contraindicated in patients with evidence of iron overload, patients with known hypersensitivity to VENOFER, and patients with anemia not caused by iron deficiency.

WARNINGS AND PRECAUTIONS

Because body iron excretion is limited and excess tissue iron can be hazardous, caution should be exercised in the administration of parenteral iron formulations, and treatment should be withheld when there is evidence of tissue iron overload. Patients receiving VENOFER (Iron Sucrose Injection, USP) require periodic monitoring of hematologic parameters, including haemoglobin, hematocrit, serum ferritin and transferrin saturation. Generally accepted guidelines recommend withholding administration of intravenous iron formulations from patients demonstrating a transferrin saturation > 50% and or serum ferritin > 800 ng/mL (see DOSAGE AND ADMINISTRATION and OVERDOSAGE). Transferrin saturation values increase rapidly after IV administration of iron sucrose; thus, serum iron values may be reliably obtained 48 hours after IV dosing.

Local Reactions: Care must be taken to avoid paravenous infiltration. If this occurs, the infusion of VENOFER should be discontinued immediately. Ice may be applied to cause local vasoconstriction and decrease fluid absorption; massage of the area should be avoided.

No long-term studies in animals have been performed to evaluate the carcinogenic potential of VENOFER. The Ames test, with or without metabolic activation, in vitro mouse lymphoma forward mutation test, mouse micronucleus test, and in vitro human lymphocyte chromosome aberration test were conducted with iron sucrose. No mutagenicity or genotoxicity was demonstrated.

Hypotension has been reported frequently in hemodialysis dependent chronic kidney disease patients receiving intravenous iron. Hypotension also has been reported in non-dialysis dependent (NDD-CK) and peritoneal dialysis dependent (PDD-CK) chronic disease kidney patients receiving intravenous iron. Hypotension following administration of VENOFER may be related to the rate of administration and total dose administered. Caution should be taken to administer VENOFER according to recommended guidelines. See DOSAGE AND ADMINISTRATION.

Serious hypersensitivity reactions have been rarely reported in patients receiving VENOFER. No life-threatening hypersensitivity reactions were observed in pivotal studies, although there were several cases of mild to moderate hypersensitivity reactions characterized by wheezing, dyspnea, hypotension, rash and/or pruritus in these studies. Anaphylactoid reactions have been reported in worldwide spontaneous post-marketing reports (see ADVERSE REACTIONS).

VENOFER at IV doses up to 15 mg iron/kg/dose [about 10 times the maximum recommended human dose for a 70 kg person] given three times a week was found to have no effect on fertility and reproductive performance of male and female rats.

Pregnant Women:

Teratology studies performed in rats at IV doses up to 13 mg iron/kg/day (more than 9 times the maximum recommended human dose for a 70 kg person) and rabbits at IV doses up to 13 mg iron/kg on alternate days (approximately 9 times the maximum recommended human dose for a 70 kg person) have not revealed definitive evidence of impaired fertility. Fetal growth effects at these doses appeared related to low maternal food consumption and low body weight gain. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, VENOFER should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

When iron sucrose was administered at deliberate overdoses to rabbit dams (up to 215 mg/kg/day) marked fetal/placental iron overload was noted. It is unlikely that significant fetal iron overload would occur in iron deficient pregnant women receiving therapeutic doses of VENOFER to correct iron deficiency (see General).

Nursing Women:

VENOFER is excreted in the milk of rats. It is not known whether VENOFER is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when VENOFER is administered to nursing women.

Pediatrics

: The safety and effectiveness of VENOFER in pediatric patients has not been established. In a country where VENOFER is available for use in children, at a single site, five premature infants (weight less than 1,250 g) developed necrotizing enterocolitis and two of the five expired during or following a period when they received VENOFER, several other medications and erythropoietin. Necrotizing enterocolitis may be a complication of prematurity in very low birth weight infants. No causal relationship to VENOFER or any other drugs could be established.

Geriatrics (> 65 years of age)

: Clinical studies with VENOFER have not identified differences in unintended responses between elderly and younger patients. Nevertheless, dose selection for an elderly patient should be cautious, usually starting with lower doses, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

ADVERSE REACTIONS

Adverse Drug Reaction Overview

The most common treatment-related adverse events were dysgeusia, hypotension [not otherwise specified (NOS)], nausea, and dizziness. In the HDD-CKD clinical indication group, the most common treatment-related adverse event was hypotension NOS. In the NDD-CKD clinical indication group, the most common treatment- related adverse events were dysgeusia in the VENOFER group. In the PDD-CKD clinical indication group, the most common event in the VENOFER group was diarrhea. The most common treatment-emergent adverse events related to study drug were hypotension NOS in the 100 mg dose group, dysgeusia in the 200 mg dose group, diarrhea NOS in the 300 mg and 400 mg dose groups, and peripheral edema, dizziness, and hypotension NOS in the 500 mg dose group. No dose-related trends were noted for serious adverse events or premature discontinuations due to adverse events. No clinically important incidence of hypersensitivity/allergic reaction was observed in the clinical studies. Hypotension has been reported frequently in hemodialysis patients receiving IV iron.

Clinical Trial Adverse Drug Reactions

Because clinical trials are conducted under very specific conditions the adverse reaction rates observed in the clinical trials may not reflect the rates observed in practice and should not be compared to the rates in the clinical trials of another drug. Adverse drug reaction information from clinical trials is useful for identifying drug-related adverse events and for approximating rates.

Adverse Events observed in all treated populations

The frequency of adverse events associated with the use of VENOFER has been documented in six randomized clinical trials involving 231 hemodialysis dependent, 139 non-dialysis dependent, and 75 peritoneal dialysis dependent patients; and in two post-marketing safety studies involving 1051 hemodialysis dependent patients for a total of 1496 patients. In addition, over 2000 patients treated with VENOFER have been reported in the medical literature. Treatment-emergent adverse events reported by >= 2% of treated patients in the randomized clinical trials, whether or not related to VENOFER administration, are listed by indication in Table 1.

Table 1 - Most Common Treatment-Emergent Adverse Events Reported in >= 2% of Patients by Clinical Indication (Multidose Safety Population)

Adverse Events (Preferred Term)	HDD-CKD	NDD-CKD		PDD-CKD
	VENOFER	VENOFER	Oral Iron	VENOFER	EPO Only
	(N=231)	(N=139)	(N=139)	(N=75)	(N=46)
	%	%	%	%	%
Subjects with any adverse event	78.8	76.3	73.4	72.0	65.2
Ear and Labyrinth Disorders Ear pain	0	2.2	0.7	0	0
Eye Disorders Conjunctivitis	0.4	0	0	2.7	0
Gastrointestinal Disorders	3.5	1.4	2.9	4.0	6.5
Abdominal pain NOS	3.5	1.4	2.9	4.0	6.5
Constipation	1.3	4.3	12.9	4.0	6.5
Diarrhea NOS	5.2	7.2	10.1	8.0	4.3
Dysgeusia	0.9	7.9	0	0	0
Nausea	14.7	8.6	12.2	5.3	4.3
Vomiting NOS	9.1	5.0	8.6	8.0	2.2
General Disorders and	2.2	0.7	2.2	2.7	0
Administration Site Conditions
Asthenia
Chest pain	6.1	1.4	0	2.7	0
Edema NOS	0.4	6.5	6.5	0	2.2
Fatigue	1.7	3.6	5.8	0	4.3
Feeling abnormal	3.0	0	0	0	0
Infusion site burning	0	3.6	0	0	0
Injection site extravasation	0	2.2	0	0	0
Injection site pain	0	2.2	0	0	0
Peripheral edema	2.6	7.2	5.0	5.3	10.9
Pyrexia	3.0	0.7	0.7	1.3	0
Infections and Infestations	0	0	0	4.0	8.7
Catheter site infection	0	0	0	4.0	8.7
Nasopharyngitis	0.9	0.7	2.2	2.7	2.2
Peritoneal infection	0	0	0	8.0	10.9
Sinusitis NOS	0	0.7	0.7	4.0	0
Upper respiratory tract infection NOS	1.3	0.7	1.4	2.7	2.2
Urinary tract infection NOS	0.4	0.7	5.0	1.3	2.2
Injury, Poisoning and Procedural Complications Graft complication	9.5	1.4	0	0	0
Investigations	0.4	2.2	2.2	0	0
Cardiac murmur NOS	0.4	2.2	2.2	0	0
Fecal occult blood positive	0	1.4	3.6	2.7	4.3
Metabolism and Nutrition Disorders	3.0	1.4	0.7	1.3	0
Fluid overload	3.0	1.4	0.7	1.3	0
Gout	0	2.9	1.4	0	0
Hyperglycemia NOS	0	2.9	0	0	2.2
Hypoglycemia NOS	0.4	0.7	0.7	4.0	0
Adverse Events (Preferred Term)	HDD-CKD	NDD-CKD		PDD-CKD
Adverse Events (Preferred Term)	VENOFER (N=231) %	VENOFER (N=139) %	Oral Iron (N=139) %	VENOFER (N=75) %	EPO Only (N=46) %
Musculoskeletal and Connective	3.5	1.4	2.2	4.0	4.3
Tissue Disorders
Arthralgia
Arthritis NOS	0	0	0	0	4.3
Back pain	2.2	2.2	3.6	1.3	4.3
Muscle cramp	29.4	0.7	0.7	2.7	0
Myalgia	0	3.6	0	1.3	0
Pain in extremity	5.6	4.3	0	2.7	6.5
Nervous System Disorders	6.5	6.5	1.4	1.3	4.3
Dizziness	6.5	6.5	1.4	1.3	4.3
Headache	12.6	2.9	0.7	4.0	0
Hypoesthesia	0	0.7	0.7	0	4.3
Respiratory, Thoracic and	3.0	2.2	0.7	1.3	0
Mediastinal Disorders
Cough
Dyspnea	3.5	3.6	0.7	1.3	2.2
Dyspnea exacerbated	0	2.2	0.7	0	0
Nasal congestion	0	1.4	2.2	1.3	0
Pharyngitis	0.4	0	0	6.7	0
Rhinitis allergic NOS	0	0.7	2.2	0	0
Skin and Subcutaneous Tissue	3.9	2.2	4.3	2.7	0
Disorders
Pruritus
Rash NOS	0.4	1.4	2.2	0	2.2
Vascular Disorders	6.5	6.5	4.3	8.0	6.5
Hypertension NOS	6.5	6.5	4.3	8.0	6.5
Hypotension NOS	39.4	2.2	0.7	2.7	2.2

Treatment-emergent adverse events reported in >=2% of patients by dose group are shown in Table 2.

Table 2. Most Common Treatment-Emergent Adverse Events Reported in > 2% of Patients by Dose Group (Multidose Safety Population)
Adverse Events (Preferred Term )	HDD-CKD	NDD-CKD		PDD-CKD
	100 mg	200 mg	500 mg	300 mg for 2
	(N=231)	(N=109)	(N=30)	doses followed
	%	%	%	by 400 mg
				for 1 dose
				(N= 75)
				%
Subjects with any adverse event	78.8	75.2	80.0	72.0
Ear and Labyrinth Disorders Ear pain	0	0.9	6.7	0
Eye Disorders Conjunctivitis	0.4	0	0	2.7
Gastrointestinal Disorders	3.5	1.8	0	4.0
Abdominal pain NOS *	3.5	1.8	0	4.0
Constipation	1.3	3.7	6.7	4.0
Diarrhea NOS	5.2	6.4	10.0	8.0
Dysgeusia	0.9	9.2	3.3	0
Nausea	14.7	9.2	6.7	5.3
Vomiting NOS	9.1	5.5	3.3	8.0
General Disorders and	2.2	0.9	0	2.7
Administration Site Conditions
Asthenia
Chest pain	6.1	0.9	3.3	2.7
Edema NOS	0.4	7.3	3.3	0
Fatigue	1.7	4.6	0	0
Feeling abnormal	3.0	0	0	0
Infusion site burning	0	3.7	3.3	0
Injection site pain	0	2.8	0	0
Peripheral edema	2.6	5.5	13.3	5.3
Pyrexia	3.0	0.9	0	1.3
Infections and Infestations	0	0	0	4.0
Catheter site infection	0	0	0	4.0
Nasopharyngitis	0.9	0.9	0	2.7
Peritoneal infection	0	0	0	8.0
Sinusitis NOS	0	0	3.3	4
Upper respiratory tract infection	1.3	0.9	0	2.7
Injury, Poisoning and Procedural Complications Graft complication	9.5	1.8	0	0
Investigations	0.4	2.8	0	0
Cardiac murmur NOS	0.4	2.8	0	0
Fecal occult blood positive	0	1.8	0	2.7
Metabolism and Nutrition Disorders	3.0	1.8	0	1.3
Fluid overload	3.0	1.8	0	1.3
Gout	0	1.8	6.7	0
Table 2. Most Common Treatment-Emergent Adverse Events Reported in > 2% of Patients by Dose Group (Multidose Safety Population)
Adverse Events (Preferred Term )	HDD-CKD	NDD-CKD		PDD-CKD
	100 mg	200 mg	500 mg	300 mg for 2
	(N=231)	(N=109)	(N=30)	doses followed
	%	%	%	by 400 mg
				for 1 dose
				(N= 75)
				%
Hyperglycemia NOS	0	3.7	0	0
Hypoglycemia NOS	0.4	0.9	0	4.0
Musculoskeletal and Connective Tissue	3.5	0.9	3.3	4.0
Disorders
Arthralgia
Back pain	2.2	1.8	3.3	1.3
Muscle cramp	29.4	0	3.3	2.7
Myalgia	0	2.8	6.7	1.3
Pain in extremity	5.6	4.6	3.3	2.7
Nervous System Disorders	6.5	5.5	10.0	1.3
Dizziness	6.5	5.5	10.0	1.3
Headache	12.6	3.7	0	4.0
Respiratory, Thoracic and Mediastinal	3.0	0.9	6.7	1.3
Disorders
Cough
Dyspnea	3.5	1.8	10.0	1.3
Pharyngitis	0.4	0	0	6.7
Skin and Subcutaneous Tissue Disorders Pruritus	3.9	0.9	6.7	2.7
Vascular Disorders	6.5	6.4	6.7	8.0
Hypertension NOS	6.5	6.4	6.7	8.0
Hypotension NOS	39.4	0.9	6.7	2.7

*NOS=not otherwise specified

Drug related adverse events reported by >=2% of VENOFER treated patients are shown by dose group in Table 3.

Table 3. Most Common Adverse Events Related to Study Drug Reported in >= 2% of Patients by Dose Group (Multidose Safety Population)
Adverse Events ( Preferred Term)	HDD-CKD	NDD-CKD		PDD-CKD
	100 mg	200 mg	500 mg	300 mg for 2
	(N=231)	(N=109)	(N=30)	doses followed
	%	%	%	by 400 mg
				for 1 dose
				(N= 75)
				%
Subjects with any adverse event	14.7	23.9	20.0	10.7
Gastrointestinal Disorders Diarrhea NOS * Dysgeusia Nausea	0.9 0.9 1.7	0 7.3 2.8	0 3.3 0	2.7 0 1.3
General Disorders and	0	3.7	0	0
Administration Site
Conditions
Infusion site burning
Injection site pain	0	2.8	0	0
Peripheral edema	0	1.8	6.7	0
Nervous Systems Disorders	0	2.8	6.7	0
Dizziness	0	2.8	6.7	0
Headache	0	2.8	0	0
Vascular Disorders Hypotension NOS	5.2	0	6.7	0

*NOS = Not otherwise specified

Adverse Events Observed in Hemodialysis Dependent Chronic Kidney Disease (HDD- CKD) Patients

Adverse reactions, whether or not related to VENOFER administration, reported by >5% of treated patients from a total of 231 patients in HDD-CKD Studies A, B, and C were as follows: hypotension (39.4%), muscle cramps (29.4%), nausea (14.7%), headache (12.6%), graft complications (9.5%), vomiting (9.1%), dizziness (6.5%), hypertension (6.5%), chest pain (6.1%), and diarrhea (5.2%). In the first post-marketing safety study, 665 chronic hemodialysis patients were treated with VENOFER doses of 100 mg at each dialysis session for up to 10 consecutive dialysis sessions for their iron deficiency or on a weekly basis for 10 weeks for maintenance of iron stores. In this study, 72% of the patients received up to 10 doses, 27% received between 11-30 doses, and 1% received 40 to 50 doses of VENOFER. Serious adverse events and drug-related non-serious adverse events were collected. In the second post-marketing safety study, 386 hemodialysis patients were exposed to a single dose of VENOFER (100 mg IV by slow injection over 2 minutes or 200 mg IV by slow injection over 5 minutes). The mean age of patients enrolled into the two post-marketing safety studies was 59 years, with a range of 20-93 years. Males made up 60% of the population. The ethnicity of the patients enrolled in the two studies included Blacks (44%), Caucasians (41%), Hispanics (11%), Asians (3%), and others (1%). Adverse events reported by >1% of 1051 treated patients were: cardiac failure congestive, sepsis NOS and dysgeusia.

Adverse Events Observed in Non-Dialysis Dependent Chronic Kidney Disease (NDD-CKD) Patients

In Study D of 182 treated NDD-CKD patients, 91 were exposed to VENOFER. Adverse events, whether or not related to VENOFER, reported by >=5% of the VENOFER exposed patients were as follows: dysgeusia (7.7%), peripheral edema (7.7%), diarrhea (5.5%), constipation (5.5%), nausea (5.5%), dizziness (5.5%), and hypertension (5.5%). One serious related adverse reaction was reported (hypotension and shortness of breath not requiring hospitalization in a VENOFER patient). Two patients experienced possible hypersensitivity/allergic reactions (local edema/hypotension) during the study. Of the 5 patients who prematurely discontinued the treatment phase of the study due to adverse events (2 oral iron group and 3 VENOFER group), three VENOFER patients had events that were considered drug-related (hypotension, dyspnea and nausea). In an additional study of VENOFER with varying erythropoietin doses in 96 treated NDD-CKD patients, adverse events, whether or not related to VENOFER reported by >=5% of VENOFER exposed patients are as follows: diarrhea (16.5%), edema (16.5%), nausea (13.2%), vomiting (12.1%), arthralgia (7.7%), back pain (7.7%), headache (7.7%), hypertension (7.7%), dysgeusia (7.7%), dizziness (6.6%), extremity pain (5.5%), and injection site burning (5.5%). No patient experienced a hypersensitivity/allergic reaction during the study. Of the patients who prematurely discontinued the treatment phase of the study due to adverse events (2.1% oral iron group and 12.5% VENOFER group), only one patient (VENOFER group) had events that were considered drug-related (anxiety, headache, and nausea). Ninety-one (91) patients in this study were exposed to VENOFER either during the treatment or extended follow-up phase.

Adverse Events Observed in Peritoneal Dialysis Dependent Chronic Kidney Disease (PDD- CKD) Patients

In Study E of 121 treated PDD-CKD patients, 75 were exposed to VENOFER. Adverse events, whether or not related to VENOFER, reported by >=5% of these patients were as follows: vomiting (8.0%), diarrhea (8.0%), hypertension (8.0%), peritoneal infection (8.0%), pharyngitis (6.7%), nausea (5.3%) and peripheral edema (5.3%). The only drug related adverse reaction to VENOFER administration reported by >=2% of patients was diarrhea (2.7%). No serious drug related adverse reactions were reported during the treatment phase of study. Two VENOFER patients experienced a moderate hypersensitivity / allergic reaction (rash or swelling/itching) during the study. Three patients in the VENOFER study group discontinued study treatment due to adverse events (cardiopulmonary arrest, peritonitis, myocardial infarction, hypertension) which were considered to be not drug-related.

Hypersensitivity Reactions: WARNINGS AND PRECAUTIONS

See

In clinical studies, several patients experienced hypersensitivity reactions presenting with wheezing, dyspnea, hypotension, rashes, or pruritus. Serious episodes of hypotension occurred in 2 patients treated with VENOFER at a dose of 500 mg. One hundred thirty (11%) of the 1151 patients evaluated in the 4 U.S. trials in HDD-CKD patients (studies A, B and the two post marketing studies) had other prior intravenous iron therapy and were reported to be intolerant (defined as precluding further use of that iron product). When these patients were treated with VENOFER there were no occurrences of adverse events that precluded further use of VENOFER.

Post-Market Adverse Drug Reactions

Hypersensitivity Reactions: WARNINGS AND PRECAUTIONS

See

From the post-marketing spontaneous reporting system, there were 108 reports of anaphylactoid reactions including patients who experienced serious or life-threatening reactions (anaphylactic shock, loss of consciousness or collapse, bronchospasm with dyspnea, or convulsion) associated with VENOFER administration between 1992 and August, 2005 based on estimated use in more than 4.6 million patients. Among the 517,736 patients (estimated on the basis of 10,354,715 ampoules sold) who received VENOFER between September 1, 2005 and February 28, 2006 through market exposure, 61 patients were reported to have experienced 104 adverse reactions considered at least "possibly related" to VENOFER. A review of all the symptoms concluded that 90 symptoms are listed, 38 serious and 52 non-serious; 14 symptoms are unlisted, 5 serious and 9 non-serious. Considering the number of patients exposed to VENOFER, the number of adverse events at least possibly related to the product has been very limited. There was a moderate decrease in the frequency of unlisted symptoms and no changes in the nature of the listed ones. During this period no overdose of misuse have been reported. Regarding the serious and listed cases: no particular change or trend in severity, outcome or involved populations could be observed. A total of 38 adverse reactions were reported in 18 patients. No reaction was considered to be life threatening. The symptoms observed were: dysponea (5), hypotension (4), pyrexia (2), injection site reaction (2), erythema (2), rash (2), arthralgia (2), chills (1), circulatory collapse (1), nausea (1), vomiting (1), tachycardia (1), myalgia (1), malaise (1), abdominal pain (1), exanthema (1), oedema peripheral (1), urticaria (1), loss of consciousness (1), dizziness (1), back pain (1), headache (1). There was no particular evolution regarding the non-serious and listed events. A total of 51 adverse symptoms were reported in 37 different patients. The symptoms observed were: urticaria (5), headache (5), dizziness (4), injection site extravasation (4), exanthem (3), tachycardia (3), chills (3), dyspnoea (3), rash (2), flushing (2), pruritus (2), pyrexia (2), paraesthesia (2), malaise (2), hypotension (1), vomiting (1), injection site pain (1), injection site reaction (1), oedema peripheral (1), arthralgia (1), myalgia (1), asthenia (1), skin discolouration (1), erythema (1). In total, eight non-serious and anaphylactoid reactions have been reported during 6-month period out of the literature. Cumulatively 116 anaphylactoid reactions have been reported out of the exposure of 5,123,048 patient years/ patient to VENOFER which results in a relative prevalence of 0.0023 %. There were 5 serious and unlisted adverse symptoms, involving 4 different patients. The symptoms observed were: asthma, pulmonary test decreased; abortion; respiratory failure; arthritis. In addition, 7 patients experienced 10 non-serious and unlisted adverse symptoms brought to the attention of the manufacturer during the period between September 1, 2005 and February 28, 2006: oedema (2), burning sensation (2), throat tightness (1), blood iron abnormal (1), arthritis (1), bone pain (1), feeling hot (1), influenza like illness (1).

DRUG INTERACTIONS

Drug interactions involving VENOFER have not been studied. Oral iron should not be administered concomitantly with parenteral iron preparations. Like other parenteral iron preparations, VENOFER may be expected to reduce the absorption of concomitantly administered oral iron preparations.

DOSAGE AND ADMINISTRATION

The dosage of VENOFER (Iron Sucrose Injection, USP) is expressed in terms of mg of elemental iron. Each 5 mL vial contains 100 mg of elemental iron (20 mg/mL). Most CKD patients will require a minimum cumulative dose of 1000 mg of elemental iron, administered over sequential sessions, to achieve a favourable haemoglobin or hematocrit response. Patients may then continue to require therapy at the lowest dose necessary to maintain target levels of haemoglobin, hematocrit and iron storage parameters within acceptable limits (ferritin, TSAT).

Non-Dialysis Dependent Chronic Kidney Disease Patients (NDD-CKD): There is limited experience with administration of an infusion of 500 mg of VENOFER

VENOFER is administered as a total cumulative dose of 1,000 mg over a 14 day period as a 200 mg slow IV injection undiluted over 2 to 5 minutes on 5 different occasions within the 14 day period.

, diluted in a maximum of 250 mL of 0.9% NaCl, over a period of 3.5 - 4 hours on day 1 and day 14; hypotension occurred in 2 of 30 patients treated. Patients weighing less than 70 kg may require a longer infusion time.

Hemodialysis Dependent Chronic Kidney Disease Patients (HDD-CKD):

VENOFER may be administered undiluted as a 100 mg slow intravenous injection over 2 to 5 minutes or as an infusion of 100 mg diluted in a maximum of 100mL of 0.9% NaCl over a period of at least 15 minutes per consecutive hemodialysis session for a total cumulative dose of 1000 mg.

Peritoneal Dialysis Dependent Chronic Kidney Disease Patients (PDD-CKD):

VENOFER is administered as a total cumulative dose of 1000 mg in 3 divided doses within a 28 day period: 2 infusions of 300 mg over 1.5 hours 14 days apart followed by one 400 mg infusion over 2.5 hours 14 days later. The VENOFER dose should be diluted in a maximum of 250 mL of 0.9% NaCl.

Dilution:

Parenteral Products:

When prepared as an infusion, use immediately. Do not store. Infusion rate as outlined in DOSAGE AND ADMINISTRATION.

Do not mix VENOFER with other medications or add to parenteral nutrient solutions for intravenous infusion. As with all parenteral drug products, intravenous admixtures should be inspected visually for clarity, particulate matter, precipitate, discolouration and leakage prior to administration, whenever solution and container permit. Solutions showing haziness, particulate matter, precipitate, discolouration or leakage should not be used. Discard unused portion.

OVERDOSAGE

Dosages of VENOFER (Iron Sucrose Injection, USP) in excess of iron needs may lead to the accumulation of iron in storage sites, resulting in hemosiderosis. Periodic monitoring of iron parameters such as serum ferritin and transferrin saturation may assist in recognizing iron accumulation. VENOFER should not be administered to patients with iron overload and should be discontinued when serum ferritin levels exceed usual norms (see WARNINGS AND PRECAUTIONS - General). Particular caution should be exercised to avoid iron overload where anemia unresponsive to treatment has been incorrectly diagnosed as iron deficiency anemia. Symptoms associated with overdosage or infusing VENOFER too rapidly include hypotension, headache, vomiting, nausea, dizziness, joint aches, paresthesia, abdominal and muscle pain, edema, and cardiovascular collapse. Most symptoms have been successfully treated with IV fluids, corticosteroids and/or antihistamines.

ACTION AND CLINICAL PHARMACOLOGY

VENOFER is used to replenish body iron stores in dialysis dependent and non-dialysis dependent chronic kidney disease (NDD-CKD) patients. Iron deficiency may be caused by blood loss during dialysis, increased erythropoiesis secondary to erythropoietin use, and insufficient absorption of iron from the gastrointestinal tract. Iron is essential to the synthesis of haemoglobin to maintain oxygen transport and to the function and formation of the physiologically important heme and non-heme compounds. Most dialysis patients require intravenous iron to maintain sufficient iron stores.

Following intravenous administration of VENOFER, iron sucrose is dissociated by the reticuloendothelial system into iron and sucrose. In 22 hemodialysis patients on erythropoietin therapy treated with iron sucrose at 100 mg of iron three times weekly for three weeks, significant increases in serum iron and serum ferritin and significant decreases in total iron binding capacity occurred four weeks from the initiation of iron sucrose treatment.

In healthy adults treated with intravenous doses of VENOFER, the iron component exhibits first order kinetics with an elimination half-life of 6 h, total clearance of 1.2 L/h, non-steady state apparent volume of distribution of 10.0 L, steady state apparent volume of distribution of 7.9 L, and the initial volume of distribution (Vdc) of 3.2 L. Since iron disappearance from serum depends on the need for iron in the iron stores and iron utilizing tissues of the body, serum clearance of iron is expected to be more rapid in iron deficient patients compared to healthy individuals. VENOFER is not dialyzable through CA210 (Baxter) High Efficiency or Fresenius F80A High Flux dialysis membranes. In in vitro studies, the amount of iron sucrose in the dialysate fluid was below the level of detection of the assay (less than 2 ppm). Distribution: In healthy adults treated with intravenous doses of VENOFER, the iron component appears to distribute mainly in blood and to some extent in extravascular fluid. In a study evaluating VENOFER at 100 mg of iron labelled with 52Fe/59Fe in patients with iron deficiency, it was found that a significant amount of the administered iron distributes in the liver, spleen and bone marrow. The bone marrow is an iron trapping compartment and not a reversible volume of distribution.

Metabolism and Excretion:

The sucrose component of VENOFER is eliminated mainly by urinary excretion. In a study evaluating a single intravenous dose of VENOFER containing 1510

mg of sucrose and 100 mg of iron in 12 healthy adults, 68.3% of the sucrose was eliminated in urine in 4 h and 75.4% in 24 h. About 5% of the iron was eliminated via renal excretion over 24 h.

The effects of age and gender on the pharmacokinetics of VENOFER have not been studied.

STORAGE AND STABILITY

DOSAGE FORMS, COMPOSITION AND PACKAGING

VENOFER (Iron Sucrose Injection, USP) is a brown, viscous, sterile, nonpyrogenic, aqueous solution containing 20 mg elemental iron per mL in the form of an iron(III)-hydroxide sucrose complex as the active ingredient, and water for injection. NaOH may be used to adjust the pH to 10.5 - 11.1. The sterile solution has an osmolarity of 1250 mOsmol/L. The product does not contain preservatives or dextran polysaccharides. VENOFER (Iron Sucrose Injection, USP) is available in 5 mL single dose vials, sold in boxes of Each 5 mL contains 100 mg (20 mg/mL) of elemental iron as an iron(III)-hydroxide sucrose complex in water for injection.

PHARMACEUTICAL INFORMATION

Drug Substance

Proper name: Iron Sucrose Chemical name: Iron (III)-hydroxide sucrose complex Ferric-hydroxide Sucrose Complex Saccharated Iron Oxide Molecular formula and molecular mass: Molecular formula: [Na2Fe5O8(OH) [?] 3(H2O)]n [?] m(C12H22O11) n = the degree of iron polymerization and m is the number of sucrose molecules in complex with the iron(III)-hydroxide Molecular mass: Approximately 43,200 daltons Structural formula: Exact structural formula not known. Physicochemical properties: Iron sucrose is a brown, viscous, aqueous solution with a total iron content of 3.50 - 3.90% w/w and a pH of 10.5 - 11.0.

CLINICAL TRIALS

Six clinical trials were conducted to assess the safety and efficacy of VENOFER. Five studies were conducted in the United States (516 patients) and one was conducted in South Africa (131 patients).

Study A was a multicenter, open-label, historically-controlled study in 101 hemodialysis patients (77 patients with VENOFER treatment and 24 in the historical control group) with iron deficiency anemia. Eligibility for VENOFER treatment included patients undergoing chronic hemodialysis three times weekly, receiving erythropoietin, haemoglobin concentration greater than 8.0 and less than 11.0 g/dL for at least two consecutive weeks, transferrin saturation < 20%, and serum ferritin < 300 ng/mL. The mean age of the patients in the treatment group was 65 years with the age range being 31 to 85 years of age. The erythropoietin dose was to be held constant throughout the study. The protocol did not require administration of a test dose; however, some patients received a test dose at the physician's discretion. Exclusion criteria included significant underlying disease, asthma, active inflammatory disease, or serious bacterial or viral infection. VENOFER 5 mL (one vial) containing 100 mg of elemental iron was administered through the dialysis line at each dialysis session either as slow injection or a saline diluted slow infusion for a total of 10 dialysis sessions with a cumulative dose of 1000 mg elemental iron. A maximum of 3 vials of VENOFER was administered per week. No additional iron preparations were allowed until after the Day 57 evaluation. The mean change in haemoglobin from baseline to Day 24 (end of treatment), Day 36, and Day 57 was assessed. The historical control population consisted of 24 patients with similar ferritin levels as patients treated with VENOFER, who were off intravenous iron for at least 2 weeks and who had received erythropoietin therapy with hematocrit averaging 31-36 for at least two months prior to study entry. The mean age of patients in the historical control group was 56 years, with an age range of 29 to 80 years. Patients age and serum ferritin level were similar between treatment and historical control patients. Of the 77 patients in the treatment group, 44 (57%) were male and 33 (43%) were female. The mean baseline haemoglobin and hematocrit, were higher and erythropoietin dose was lower in the historical control population than the VENOFER treated population. Patients in the VENOFER treated population showed a statistically significantly greater increase in haemoglobin and hematocrit than did patients in the historical control population. See Table 4.

* *p<0.01 and *p<0.05 compared to historical control from ANCOVA analysis with baseline haemoglobin, serum

Study B was a multicenter, open label study of VENOFER (iron sucrose injection, USP) in 23 iron deficient hemodialysis patients who had been discontinued from iron dextran due to intolerance. Eligibility criteria and VENOFER administration were otherwise identical to Study

All 23 enrolled patients were evaluated for efficacy. Statistically significant increases in mean haemoglobin (1.1+-0.2 g/dL), hematocrit (3.6+-0.6%), serum ferritin (266.3+-30.3 ng/mL) and transferrin saturation (8.7+-2.0%) were observed from baseline to end of treatment.

Study C was a multicenter, open-label, two period (treatment followed by observation period) study in iron deficient hemodialysis patients. Eligibility for this study included chronic hemodialysis patients with a haemoglobin less than or equal to 10 g/dL, a serum transferrin saturation less than or equal to 20%, and a serum ferritin less than or equal to 200 ng/mL, who were undergoing maintenance hemodialysis 2 to 3 times weekly. The mean age of the patients enrolled in this study was 41 years, with ages ranging from 16-70 years. Of 130 patients evaluated for efficacy in this study, 68 (52%) were male and 62 (48%) were female. The ethnicity breakdown of patients enrolled in this study was as follows: Caucasian (23%); Black (23%); Asian (5%); Other (mixed ethnicity) (49%). Forty-eight percent of the patients had previously been treated with oral iron. Exclusion criteria were similar to those in studies A and VENOFER, was administered in doses of 100 mg during sequential dialysis sessions until a pre-determined (calculated) total dose of iron was administered. Patients received VENOFER at each dialysis session, two to three times weekly. One hour after the start of each session, 5 mL iron sucrose (100 mg iron) in 100 mL 0.9% NaCl was administered into the hemodialysis line. A 50 mg dose (2.5 mL) was given to patients within two weeks of study entry. Patients were treated until they reached an individually calculated total iron dose based on baseline haemoglobin level and body weight. Twenty-seven patients (20%) were receiving erythropoietin treatment at study entry and they continued to receive the same erythropoietin dose for the duration of the study. Changes from baseline to observation week 2 and observation week 4 (end of study) were analyzed. The modified intention-to-treat population consisted of 131 patients. Significant (p<0.0001) increases from baseline in mean haemoglobin (1.7 g/dL), hematocrit (5%), serum ferritin (434.6 ng/mL), and serum transferrin saturation (14%) were observed at week 2 of the observation period and these values remained significantly increased (p<0.0001) at week 4 of the observation period.

Study D was a randomized, open-label, multicenter, active-controlled study of the safety and efficacy of oral iron versus intravenous iron sucrose (VENOFER) in NDD-CKD patients with or without erythropoietin therapy. Erythropoietin therapy was stable for 8 weeks prior to randomization. In the study 188 patients with NDD-CKD, transferrin saturation <=25%, ferritin <=300 ng/mL and an average baseline haemoglobin of <=11.0 g/dL were randomized to receive oral iron (325 mg ferrous sulfate three times daily for 56 days); or VENOFER (either 200 mg over 2-5 minutes 5 times within 14 days or two 500 mg infusions on Day 1 and Day 14, administered over 3.5-4 hours). Of the 188 randomized patients, 182 were treated and followed for up to 56 days. Efficacy assessments were measured on days 14, 28, 42 and 56. The mean age of the 91 treated patients in the VENOFER group was 61.6 years (range 25 to 86 years) and 64 years (range 21 to 86 years) for the 91 patients in the oral iron group. Ethnicity breakdown of the patients in the VENOFER group was as follows: Caucasian (60.4%), Black (34.1%), Hispanic (3.3%), Other (2.2%). Ethnicity breakdown for the oral iron group was: Caucasian (50.5%), Black (44.0%), Hispanic (4.4%), Other (1.1%). Patient demographic characteristics were not significantly different between the groups. A statistically significantly greater proportion of VENOFER subjects (35/79; 44.3%) compared to oral iron subjects (23/82; 28%) had an increase in haemoglobin >=1 g/dL at anytime during the study (p=0.03). In patients >=65 years of age, the proportion of subjects achieving >=1.0 g/dL increase in haemoglobin from baseline was 53% (20/38) in the VENOFER group compared to 23% (10/43) in the oral iron group. In patients <65 years of age, the proportion of subjects achieving >=1.0 g/dL increase in haemoglobin from baseline was 37% (15/41) in the VENOFER group compared to 33% (13/39) in the oral iron group. A statistically significantly greater proportion of VENOFER treated patients (31/79; 39.2%) compared to oral iron treated patients (1/82; 1.2%) had an increase in haemoglobin >=1 g/dL and ferritin >=160 ng/mL at anytime during the study (p<0.0001).

Study E was a randomized [2:1 treatment:control], open-label, multicenter study comparing PDD-CKD patients receiving erythropoietin and IV iron to PDD-CKD patients receiving erythropoietin alone without iron supplementation. In the study 126 patients with PDD-CKD, stable erythropoietin for 8 weeks, transferrin saturation <= 25%, ferritin <= 500 ng/mL and an average baseline haemoglobin of <=11.5 g/dL were randomized to receive either no iron or VENOFER (300 mg in 250 mL 0.9% NaCl over 1.5 hours on Day 1 and Day 15 and 400 mg in 250 mL 0.9% NaCl over 2.5 hours on Day 29). Of the 126 randomized patients, 121 were treated and followed for up to 71 days. Efficacy assessments were measured on days 15, 29, 43, 57 and 71. The mean age of the 75 treated patients in the VENOFER/erythropoietin group was 51.9 years (range 21 to 81 years) and 52.8 years (range 23 to 77 years) for the 46 patients in the erythropoietin alone group. Ethnicity breakdown of the patients in the VENOFER/erythropoietin group was as follows: Black (21.3%), Caucasian (36.0%), Hispanic (32.0%), Other (10.7%). Ethnicity breakdown for the erythropoietin alone group was: Black (15.2%), Caucasian (30.4%), Hispanic (43.5%), Other (10.9%). Patient demographic characteristics were not significantly different between the groups. Patients in the VENOFER/erythropoietin group had statistically significantly greater mean change from baseline to the highest haemoglobin value (1.3 g/dL) compared to subjects who received erythropoietin alone (0.6 g/dL) (p=0.0028). Additionally, statistically significantly greater mean changes from baseline to the highest ferritin and transferrin saturation values were observed for subjects who received VENOFER/erythropoietin (574.6 ng/mL and 18.2%, respectively) compared to subjects who received erythropoietin only (5.5 ng/mL and 10.4%, respectively) (p<0.0001 and p=0.0098, respectively). A statistically significant greater proportion of subjects treated with VENOFER/erythropoietin (59.1%) had an increase in haemoglobin of >=1 g/dL during the study compared to the subjects who received erythropoietin only (33.3%) (p=0.0273).

DETAILED PHARMACOLOGY

Pharmacodynamics:

Following intravenous administration of VENOFER, iron sucrose is dissociated by the reticuloendothelial system into iron and sucrose. In 22 chronic hemodialysis patients on erythropoietin therapy who completed treatment with iron sucrose at 100 mg of iron three times weekly for three weeks, significant increases in serum iron (12.8 ug/dL) and serum ferritin (266.3 ng/mL) and significant decreases in total iron binding capacity (-46.7 ug/dL) occurred four weeks from the initiation of iron sucrose treatment. Eligibility for this study included haemoglobin <11 g/dL and a ferritin < 800 ng/mL or TSAT >50%. The mean patient age in the 23 treated (10 male and 13 female) patients was 53 years (range 21-79), mean weight 70.9 kg (range of 43-112 kg), mean haemoglobin 10.4 g/dL and mean baseline serum ferritin 50.7 ng/mL.

Pharmacokinetics:

In 12 adults with iron deficiency anemia (11 females and 1 male) treated with 7 mg of iron per kg body weight (maximum 500 mg of iron) intravenous doses of VENOFER over 2.5 to 3.5 hours, the iron component had a total clearance of 0.64 L/h, steady state apparent volume of distribution of 11.4 L and the initial volume of distribution (Vdc) of 3.4 L. The total clearance was lower following the 500 mg dose than the 100 mg dose. The volumes of distributions were comparable to the results obtained in the non anemic patients. Fifty eight point one (58.1)% of the sucrose was eliminated in urine in 4 h and 90.5% in 24 h. Only 4.8% of the iron was eliminated via renal excretion over the first 24 h. By 72 hours the cumulative percentage (5.02%) was essentially unchanged. The urinary excretion of sucrose and iron was comparable to the results obtained in healthy adults following the administration of 100 mg dose. Eligibility for this study included iron deficient (ferritin < 20 ng/L and no other causes of anemia) patients with a haemoglobin between 9.0 to 13.5 g/dL in males and 9.0 to 12.5 g/dL in females with a BMI within 20% of ideal. The mean patient age was 31 years (range 18-55), mean weight 66.6 kg (range of 55-96 kg), mean BMI 24.4 (range 19.8-29) kg/m2, mean haemoglobin 11.1 g/dL and mean baseline serum ferritin 3.7 ng/mL. The ferritin level was obtained on Day 1, 2 and 3 following dosing and peaked on Day 2 with a value of 293 (SD 81) ng/mL. Since iron disappearance from serum depends on the need for iron in the iron stores and iron utilizing tissues of the body, serum clearance of iron is expected to be more rapid in iron deficient patients compared to healthy individuals.

TOXICOLOGY

Acute Toxicity

Studies in mice and rats indicated that intravenously administered iron sucrose was non-lethal at doses below 75 mg iron/kg. The LD50 of IV iron sucrose was lower for rats than mice and for male rats compared with female rats, with that of male rats being 140 mg iron/kg, and that of females 236 mg iron/kg.

Repeat-Dose Toxicity

In repeat-dosing studies in both beagles and rats, no mortality was seen at doses up to 30 mg iron/kg, administered over 1 hour three times a week for 13 weeks. Signs of toxicity from iron overload were seen in the liver, spleen and kidneys at 10 and 30 mg iron/kg. In the beagles, liver and spleen enlargement was observed in most dogs receiving the 30 mg iron/kg dose, and liver enlargement was seen in most males receiving 10 mg iron/kg. There was a clear dose-related increase in the liver weight for both sexes, with some exceptionally high individual values, particularly at 30 mg iron/kg/dose. Group mean spleen weight was increased to a statistically significant degree for both sexes receiving 30 mg iron/kg/dose. Dose-related iron deposition was observed mainly within macrophages and primarily in the liver, spleen and kidneys. In the liver, increased perivascular fibrosis and associated cellularity was seen at all doses and hepatocyte necrosis was noted at the 30 mg iron/kg dose. Extramedullary hematopoiesis was noted in the liver and spleen in dogs receiving 10 or 30 mg iron/kg/dose. The non-toxic dose in rats and dogs was considered to be 3 mg iron/kg/dose administered three times weekly [9 mg iron/kg/week]. In a dog study with a seven-year observation period, haematological changes were widely evident following red cell transfusion or IV administration of 100-300 mg iron as iron sucrose five times a week for 6-10 weeks. Liver function tests and histopathology did not demonstrate cirrhosis. Tissue iron overload was well tolerated in these dogs with the notable exception of the development of blindness in all animals due to retinal changes resembling retinitis pigmentosis beginning about 3 years after iron administration.

Mutagenicity and Genotoxicity

The Ames test, with or without metabolic activation, in vitro mouse lymphoma forward mutation test, mouse micronucleus test, and in vitro human lymphocyte chromosome aberration test were conducted with iron sucrose. No mutagenicity or genotoxicity was demonstrated.

Carcinogenicity

No long-term studies in animals have been performed to evaluate the carcinogenic potential of VENOFER.

Reproduction

REFERENCES

This leaflet is part III of a three-part "Product Monograph" published when VENOFER was approved for sale in Canada and is designed specifically for Consumers. This leaflet is a summary and will not tell you everything about VENOFER. Contact your doctor or pharmacist if you have any questions about the drug.

Only a qualified doctor or other healthcare professional should administer VENOFER. VENOFER is not intended for administration by patient.

The safety and effectiveness of VENOFER in pediatric patients has not been established.

Caution should be used when administering VENOFER to elderly patients, usually starting with the lowest dose.

VENOFER is used in the treatment of iron deficiency anemia in dialysis dependent or non-dialysis dependent chronic kidney

VENOFER is used to replenish body iron stores in dialysis dependent or non-dialysis dependent chronic kidney disease

dialysis, increased production of red blood cells secondary to erythropoietin use, and insufficient absorption of iron from the gastrointestinal tract. Iron is needed to make haemoglobin, which allows red blood cells to carry oxygen throughout the body. Most dialysis patients require intravenous iron to maintain sufficient iron stores.

iron (iron overload) in their body, patients with known hypersensitivity (allergy or sensitivity) to VENOFER, and patients with anemia not caused by iron deficiency.

Drug interactions involving VENOFER have not been studied. Oral iron should not be administered together with other injectable iron preparations. Like other injectable iron preparations, VENOFER may reduce the absorption of oral iron preparations.

Chronic Kidney Disease Patients not on Dialysis: VENOFER is administered as a total cumulative dose of 1000 mg over a 14 day period as a 200 mg slow intravenous injection on 5 different occasions within the 14 day period or as an infusion of 500 mg of VENOFER over a period of 4 hours on day 1 and day 14; patients weighing less than 70 kg may require longer infusion times.

Hemodialysis Patients: VENOFER is administered as a 100 mg slow intravenous injection or as an infusion of 100 mg per consecutive hemodialysis session for a total cumulative dose of 1000 mg.

Peritoneal Dialysis Patients: VENOFER is administered as a total cumulative dose of 1000 mg in 3 divided doses within a 28 day period: 2 infusions of 300 mg over 1.5 hours 14 days apart followed by one 400 mg infusion over 2.5 hours 14 days later.

Symptoms associated with overdosage or infusing VENOFER too rapidly include low blood pressure, headache, vomiting, nausea, dizziness, joint aches, a burning, pricking or tingling feeling,

Common side effects that may occur include: nausea, dizziness, headache, vomiting, diarrhea, abdominal pain, fever, chest pain, muscle cramps (especially leg cramps). If these become bothersome, consult your doctor.

Very rare cases of severe, sometimes life threatening allergic reactions (loss of consciousness, collapse, difficulty breathing or convulsions) and cases of severe low blood pressure (hypotension) have been reported with the use of VENOFER. Only a qualified doctor or other healthcare professional should administer VENOFER. VENOFER is not intended for administration by patient.

To monitor drug safety, Health Canada collects information on serious and unexpected effects of drugs. If you suspect you have had a serious or unexpected reaction to this drug you may notify Health Canada by:

NOTE: Before contacting Health Canada, you should contact your physician or pharmacist.

This document plus the full product monograph, prepared for health professionals can be found at: http://www.luitpold.com or http://www.americanregent.com or by contacting the sponsor, Luitpold Pharmaceuticals, Incorporated, at:

This is not a complete list of side effects. For any unexpected effects while taking VENOFER, contact your doctor or pharmacist.

Route of Administration	Dosage Form / Strength	Clinically Relevant Nonmedicinal Ingredients
intravenous	5 mL Single Dose Vials, 20 mg elemental iron/mL	water for injection For a complete listing see Dosage Forms, Composition and Packaging section.

Dose (mg Fe)	Nominal Concentration per mL	Volume of Venofer (r) to be Added to Diluent	Volume of Diluent
Hemodialysis Dependent Chronic Kidney Disease Patients (HDD-CKD):
100 mg	1 mg/mL (when the maximum of 100 mL 0.9% NaCl is used).	5 mL	Maximum 100 mL 0.9% NaCl
Non-Dialysis Dependent Chronic Kidney Disease Patients (NDD-CKD):
500 mg	2 mg/mL (when the maximum of 250 mL 0.9% NaCl is used).	25 mL	Maximum 250 mL 0.9% NaCl
Peritoneal Dialysis Dependent Chronic Kidney Disease Patients (PDD-CKD):
300 mg	1.2 mg/mL (when the maximum of 250 mL 0.9% NaCl is used).	15 mL	Maximum 250 mL 0.9% NaCl
400 mg	1.6 mg/mL (when the maximum of 250 mL 0.9% NaCl is used).	20 mL	Maximum 250 mL 0.9% NaCl

Efficacy parameters	End of treatment		2 week follow-up		5 week follow-up
Efficacy parameters	VENOFER (n=69)	Historical Control (n=18)	VENOFER (n=73)	Historical Control (n=18)	VENOFER (n=71)	Historical Control (n=15)
Hemoglobin (g/dL)	1.0+-0.12 * *	0.0+-0.21	1.3+-0.14 * *	-0.6+-0.24	1.2+-0.17 *	-0.1+-0.23
Hematocrit (%)	3.1+-0.37 * *	-0.3+-0.65	3.6+-0.44 * *	-1.2+-0.76	3.3+-0.54	0.2+-0.86

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effect		Talk with your doctor or pharmacist		Stop taking drug and call your doctor or pharmacist
		Only if severe	In all cases
Serious Side Effects	Severe allergic reactions, sometimes life threatening with symptoms such as difficulty breathing, convulsion, collapse, itching, rash. Low blood pressure, with symptoms such as fainting, weakness.		U U

PART I: HEALTH PROFESSIONAL INFORMATION 3

PART II: SCIENTIFIC INFORMATION 19

PART III: CONSUMER INFORMATION. 27

R

PART I: HEALTH PROFESSIONAL INFORMATION SUMMARY PRODUCT INFORMATION

INDICATIONS AND CLINICAL USE

Geriatrics (> 65 years of age):

Pediatrics:

CONTRAINDICATIONS

WARNINGS AND PRECAUTIONS

Pregnant Women:

Nursing Women:

Pediatrics

Geriatrics (> 65 years of age)

ADVERSE REACTIONS

Adverse Events observed in all treated populations

Adverse Events Observed in Hemodialysis Dependent Chronic Kidney Disease (HDD- CKD) Patients

Adverse Events Observed in Non-Dialysis Dependent Chronic Kidney Disease (NDD-CKD) Patients

Adverse Events Observed in Peritoneal Dialysis Dependent Chronic Kidney Disease (PDD- CKD) Patients

Hypersensitivity Reactions: WARNINGS AND PRECAUTIONS

Hypersensitivity Reactions: WARNINGS AND PRECAUTIONS

DRUG INTERACTIONS

DOSAGE AND ADMINISTRATION

Non-Dialysis Dependent Chronic Kidney Disease Patients (NDD-CKD): There is limited experience with administration of an infusion of 500 mg of VENOFER

Hemodialysis Dependent Chronic Kidney Disease Patients (HDD-CKD):

Peritoneal Dialysis Dependent Chronic Kidney Disease Patients (PDD-CKD):

Dilution:

Parenteral Products:

OVERDOSAGE

ACTION AND CLINICAL PHARMACOLOGY

Metabolism and Excretion:

STORAGE AND STABILITY

DOSAGE FORMS, COMPOSITION AND PACKAGING

PHARMACEUTICAL INFORMATION

Drug Substance

CLINICAL TRIALS

DETAILED PHARMACOLOGY

Pharmacodynamics:

Pharmacokinetics:

TOXICOLOGY

Acute Toxicity

Repeat-Dose Toxicity

Mutagenicity and Genotoxicity

Carcinogenicity

Reproduction

REFERENCES