MILRINONE 1 MG/ML SOLUTION FOR INJECTION OR INFUSION
Active substance(s): MILRINONE
NAME OF THE MEDICINAL PRODUCT
Milrinone 1 mg/ml Solution for injection or infusion
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains 1 mg of the active substance milrinone.
Each 10 ml ampoule contains 10 mg milrinone.
This medicinal product contains less than 1 mmol sodium (23 mg) per dose, i.e.
essentially ‘sodium- free’.
For a full list of excipients, see section 6.1.
Solution for injection or infusion.
Clear, colourless to pale yellow liquid free from visible particle.
Osmolarity: Between 230 mOsmol/L and 330 mOsmol/L
pH: Between 3.20 and 4.00
Milrinone 1 mg/ml Solution for injection or infusion is indicated for the short-term
treatment (48 hours) of severe congestive heart failure unresponsive to conventional
maintenance therapy (glycosides, diuretics, vasodilators and/or angiotensin
converting enzyme (ACE) inhibitors).
In the paediatric population Milrinone 1 mg/ml Solution for injection or infusion is
indicated for the short-term treatment (up to 35 hours) of severe congestive heart
failure unresponsive to conventional maintenance therapy (glycosides, diuretics,
vasodilators and/or angiotensin converting enzyme (ACE) inhibitors), and for the
short-term treatment (up to 35 hours) of paediatric patients with acute heart failure,
including low output states following cardiac surgery.
Posology and method of administration
Posology Careful monitoring should be maintained during milrinone therapy
including blood pressure, heart rate, clinical state, electro-cardiogram, fluid balance,
electrolytes and renal function (i.e. serum creatinine)(see section 4.4). Facilities must
be available for immediate treatment of potential adverse cardiac effects (e.g. lifethreatening ventricular arrhythmias). The infusion rate should be adjusted according
to haemodynamic response.
Adults: Milrinone 1 mg/ml Solution for injection or infusion should be given as a
loading dose of 50µg/kg administered over a period of 10 minutes usually followed
by a continuous infusion at a dosage titrated between 0.375µg/kg/min and
0.75µg/kg/min (standard 0.5 µg/kg/min) according to haemodynamic and clinical
response and the possible onset of undesirable effects such as hypotension and
The total dose should not exceed 1.13 mg/kg/day total dose which corresponds to an
infusion rate of 45.0 µg/kg/hr.
The following provides a guide to maintenance infusion delivery rate based upon a
solution containing milrinone 200µg/ml prepared by adding 40ml diluent per 10ml
ampoule 0.45% saline, 0.9% saline or 5% glucose may be used as diluents.
Solutions of different concentrations may be used according to patient fluid
requirements. The duration of therapy should depend upon the patient's response
Renal Impairment: Dosage adjustment required. Dosage adjustment in patients with
renal impairment is based on data obtained from patients with common renal
impairment but without congestive heart failure, who show significant increases to
the terminal elimination half-life of milrinone. The loading dose is not affected, but a
reduction in the maintenance infusion rates may be necessary depending on the
severity (creatinine clearance) of the renal impairment (see table below):.
Milrinone 1 mg/ml
Solution for injection
Delivery Rate (for a
solution containing 200 µg
milrinone per ml)
Older people: Experience so far suggests that no special dosage recommendations are
necessary in patients with normal renal function. Renal clearance may be reduced in
older people, lower Milrinone 1 mg/ml Solution for injection or infusion doses may
be required in such cases.
In published studies selected doses for infants and children were:
• Intravenous loading dose: 50 to 75 µg/kg administered over 30 to 60 minutes.
• Intravenous continuous infusion: To be initiated on the basis of hemodynamic
response and the possible onset of undesirable effects between 0.25 to 0.75 µg/kg/min
for a period up to 35 hours.
In clinical studies on low cardiac output syndrome in infants and children under 6
years of age after corrective surgery for congenital heart disease 75 µg/kg loading
dose over 60 minutes followed by a 0.75 µg/kg/min infusion for 35 hours
significantly reduced the risk of development of low cardiac output syndrome.
Results of pharmacokinetic studies (see section 5.2) have to be taken into
Due to lack of data the use of milrinone is not recommended in paediatric population
with renal impairment (for further information please see section 4.4).
Patent ductus arteriosus:
If the use of milrinone is desirable in preterm or term infants at risk of/with
patent ductus arteriosus, the therapeutic need must be weighed against potential risks
(see section 4.4, 4.8, 5.2, and 5.3).
Method of administration
For slow intravenous administration. To avoid local irritation, as large a vein as
possible should be punctured. Extravascular injection must be avoided.
Milrinone 1 mg/ml Solution for injection or infusion may not be mixed with other
diluents as stated above (see section 6.2). Solutions of different concentrations may
be used according to patient fluid requirements. After dilution the solution is a clear
and colourless liquid free from visible particle..
The duration of therapy should depend upon the patient's response but should not
exceed 48 hours due to a lack of evidence of safety and efficacy in long-term
treatment of congestive heart failure (see section 4.4).
• Hypersensitivity to milrinone (active substance) or any of the excipients listed in
• Severe hypovolaemia.
Special warnings and precautions for use
Careful monitoring should be maintained during therapy with Milrinone 1 mg/ml
Solution for injection, or infusion including blood pressure, heart rate, clinical state,
electro-cardiogram, fluid balance, electrolytes and renal function (i.e. serum
creatinine). Facilities must be available for immediate treatment of potential adverse
cardiac effect (e.g. life threatening ventricular arrhythmias).
In patients with severe obstructive aortic or pulmonary valvular disease, or
hypertrophic subaortic stenosis (KMP), Milrinone 1 mg/ml Solution for injection or
infusion should not be used in lieu of surgical relief of the obstruction. As with other
drugs with inotropic / vasodilator properties, it may aggravate outflow obstruction in
Milrinone is not recommended immediately following acute myocardial infarction
until safety and efficacy have been established in this situation. Use of positive
inotropes such as milrinone in the acute phase of post myocardial infarction may lead
to an undesirable increase in myocardial oxygen consumption (MVO2).
There is a possibility of an increased ventricular response rate in patients with atrial
flutter or fibrillation. In these patients, prior digitalisation or treatment with other
agents to prolong atrio-ventricular node conduction time should be considered, as
milrinone produces a slight enhancement in A-V node conduction.
Supraventricular and ventricular arrhythmias have been observed in the high risk
population treated with milrinone. In some patients, an increase in ventricular ectopy
including non-sustained ventricular tachycardia has been observed.
Patients, especially those with complex ventricular arrhythmias, should therefore be
kept under continuous ECG and clinical monitoring during Milrinone 1 mg/ml
Solution for injection or infusion therapy and the dosage should be carefully adjusted.
If prior vigorous diuretic therapy is suspected of having caused significant decreases
in cardiac filling pressure Milrinone 1 mg/ml Solution for injection or infusion should
be cautiously administered while monitoring blood pressure, heart rate and clinical
Fluid and electrolyte changes, as well as serum creatinine levels should be carefully
monitored during treatment. Improvement in cardiac output with resultant diuresis
may necessitate a reduction in the dose of diuretic.
Potassium loss due to excessive diuresis may predispose digitalised patients to
arrhythmias. Therefore, hypokalaemia should be corrected by potassium
supplementation in advance of, or during, the use of Milrinone 1 mg/ml Solution for
injection or infusion.
Milrinone may induce hypotension as a consequence of its vasodilatory activity;
caution should therefore be exercised when Milrinone 1 mg/ml Solution for injection
or infusion is administered to patients who are hypotensive prior to treatment. In
patients showing excessive decreases in blood pressure after milrinone
administration, the treatment should be discontinued until the hypotensive effect has
been resolved and then resumed, if necessary, at a lower rate of infusion.
Decrease in haemoglobin, including anaemia, often takes place in the setting of
cardiac failure. Due to the risk of thrombocytopenia or anaemia, careful monitoring of
the corresponding laboratory parameters is required in patients with decreased platelet
count or decreased haemoglobin.
There is no experience in controlled trials with infusions of milrinone for periods
exceeding 48 hours.
Cases of infusion site reaction have been reported with Milrinone 1 mg/ml Solution
for injection or infusion (see Section 4.8). Consequently, careful monitoring of the
infusion site should be maintained to avoid possible extravasation.
This medicinal product contains less than 1 mmol sodium (23 mg) per dose, i.e.
essentially ‘sodium- free’.
Use in Older people: There are no special recommendations for older people. No agerelated effects on the incidence of adverse reactions have been observed. Controlled
pharmacokinetic studies have not shown changes in the pharmacokinetic profile of
milrinone in older people.
The following should be considered in addition to the warnings and precautions
described for adults:
In neonates, monitoring should include heart rate and rhythm, systemic arterial blood
pressure via umbilical artery catheter or peripheral catheter, central venous pressure,
cardiac index, cardiac output, systemic vascular resistance, pulmonary artery
pressure, and atrial pressure. Laboratory values that should be followed are platelet
count, serum potassium, liver function, and renal function. Frequency of assessment
is determined by baseline values, and it is necessary to evaluate the neonate's
response to changes in therapy.
Literature revealed that in paediatric patients with impaired renal function, there were
marked impairment of milrinone clearance and clinically significant side effects, but
the specific creatinine clearance at which doses must be adjusted in paediatric patients
is still not clear, therefore the use of milrinone is not recommended in this population
(see section 4.2).
In paediatric patients milrinone should be initiated only if the patient is
Caution should be exercised in neonates with risk factors of intraventricular
haemorrhage (i.e. preterm infant, low birth weight) since milrinone may induce
thrombocytopenia. In clinical studies in paediatric patients, risk of thrombocytopenia
increased significantly with duration of infusion. Clinical data suggest that milrinonerelated thrombocytopenia is more common in children than in adults (see section 4.8).
In clinical studies milrinone appeared to slow the closure of the ductus arteriosus in
paediatric population. Therefore, if the use of milrinone is desirable in preterm or
term infants at risk of/with patent ductus arteriosus, the therapeutic need must be
weighed against potential risks (see section 4.2, 4.8, 5.2, and 5.3).
Use in patients with renal impairment
In patients with severe renal impairment, dosage adjustment is required (see section
Interaction with other medicinal products and other forms of interaction
Fluid and electrolyte changes, as well as serum creatinine levels, should be carefully
monitored during treatment with milrinone. The effect of milrinone and diuretics may
be mutually potentiated. Additive, diuretic and hypokalaemic effects have been
observed. Improvement in cardiac output and consequently, diuresis, may require
reduction in the dose of a diuretic agent. Potassium loss due to excessive diuresis may
predispose digitalised patients to arrhythmias. Therefore, hypokalaemia should be
corrected by potassium supplementation in advance of, or during milrinone use. If
inotropic agents (e.g. dobutamine) are co-administered, the positive inotropic effects
may be potentiated.
Concomitant administration of inotropic agents increases the positive inotropic
For incompatibilities, reference is made to section 6.2.
Fertility, pregnancy and lactation
Use in Pregnancy
Although animal studies have not revealed evidence of drug-induced fetal damage or
other deleterious effects on reproductive function, the safety of milrinone in human
pregnancy has not yet been established. It should be used during pregnancy only if
the potential benefit justifies the potential risk to the fetus.
Use in Breast feeding
There is insufficient information on the excretion of milrinone in human milk. A
decision must be made whether to discontinue breast-feeding or to discontinue
milrinone therapy taking into account the benefit of breast feeding for a child and the
benefit of therapy for the woman.
There were no effects on fertility in male and female rats (see section 5.3).
Effects on ability to drive and use machines
No studies on the effect on the ability to drive and use machines have been
Adverse reactions have been ranked under heading of system-organ class and
frequency using the following convention: very common (≥1/10); common (≥1/100to
<1/10); uncommon (≥1/1,000 to ,<1/100); rare (≥1/10,000 to <≤1/1,000); very rare
(<1/10,000); not known (cannot be estimated from the available data).
Blood and the lymphatic system disorders:
• Uncommon: Thrombocytopenia
• Not known: reduction of red blood count and/or haemoglobin concentration
Immune system disorders:
• Very rare: Anaphylactic shock
Metabolism and nutrition disorders:
• Uncommon: Hypokalaemia
Nervous system disorders:
• Common: Headaches, usually mild to moderate in severity
• Uncommon: Tremor
- Ventricular ectopic activity
- Non sustained or sustained ventricular Tachycardia
- Supraventricular arrhythmias1
1 The incidence of arrhythmias has not been related to dose or plasma levels of
milrinone. Life threatening arrhythmias are often found to be associated with
underlying risk factors such as pre-existing arrhythmias, metabolic abnormalities (e.g.
hypokalaemia), elevated serum digoxin levels or catheter insertion. Clinical data
suggest that milrinone-related arrhythmias are less common in children than in adults.
- Ventricular fibrillation
- Angina/chest pain
• Very rare: Torsades de pointes
Respiratory, thoracic and mediastinal disorders:
• Very rare: Bronchospasm
• Uncommon: Liver function tests abnormal
Skin and subcutaneous tissue disorders:
• Very rare: Skin reactions such as rash
General disorders and administration site conditions:
• Not known: Infusion site reaction
Nervous system disorders
Not known: intraventricular haemorrhage (see section 4.4)
Congenital, familial, and genetic disorders
Not known: patent ductus arteriosus*** (see section 4.2, 4.4, 5.2, and 5.3)
***The critical consequences of the patent ductus arteriosus are related to a
combination of pulmonary overcirculation with consecutive pulmonary oedema and
haemorrhage and of reduced organ perfusion with consecutive intraventricular
haemorrhage and necrotizing enterocolitis with possible fatal outcome as described in
Long-term safety data for paediatric population are not yet available.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is
important. It allows continued monitoring of the benefit/risk balance of the medicinal
product. Healthcare professionals are asked to report any suspected adverse reactions
via the national reporting system (see details below)
Yellow Card Scheme
Overdose of intravenous Milrinone 1mg/ml Solution for injection or infusion may
produce hypotension (because of its vasodilatory effect) and cardiac arrhythmia. If
this occurs, Milrinone 1 mg/ml Solution for injection or infusion administration
should be reduced or temporarily discontinued until the patient's condition stabilises.
No specific antidote is known, but general measures for circulatory support should be
Pharmacotherapeutic group: Cardiac therapy; Phosphodiesterase inhibitor, ATC code:
Milrinone is a positive inotropic and vasodilator substance with little chronotropic,
bathmotropic and dromotropic activity.
It differs from both digitalis glycosides and catecholamines in terms of its structure
and mode of action.
At inotropic and vasorelaxant concentrations, milrinone is a selective inhibitor of the
peak III cAMP phosphodiesterase isoenzyme in cardiovascular muscles. In the
myocardial cell, this inhibitory effect leads to a cAMP-mediated increase in
intracellular ionised calcium and myocardial contractility, as well as a cAMPdependent phosphorylation of contractile proteins. In the vascular muscle cell, there is
a cAMP-mediated decrease in intracellular ionised calcium and hence a relaxation of
vascular muscles. Further experimental findings indicate that milrinone is not a betareceptor agonist and, unlike digitalis glycosides, it does not inhibit Na+/Ka+-ATPase
Clinical studies in patients with heart failure have shown that milrinone, depending
on the dose and its plasma concentration, leads to an increase in the maximum rate of
increase of left-ventricular pressure. Studies in healthy subjects have shown that the
slope of the left-ventricular pressure/volume relationship increases during milrinone
therapy. This indicates a direct inotropic effect of the substance. In patients with heart
failure, milrinone also led to a dose-related and plasma concentration-related increase
in forearm blood flow, indicating a direct vasodilator effect on the arteries.
In addition to the increase in myocardial contractility, milrinone improves diastolic
function, as demonstrated by improvements in left-ventricular diastolic relaxation.
In patients with impaired myocardial function, injection of milrinone within the usual
dosage range led to a rise in the cardiac index and a reduction in pulmonary capillary
pressure and vascular resistance. The heart rate increased by 3% to 10%, depending
on the dose. Mean arterial blood pressure fell dose-dependently by 5% to 17%. The
haemodynamic improvements correlated with the dose and milrinone plasma
concentration and were accompanied by an improvement in clinical symptoms. The
vast majority of patients showed improvements in haemodynamic parameters within
five to fifteen minutes after the start of treatment.
Milrinone also shows a positive inotropic effect in digitalised patients. There are no
indications that milrinone increases the toxicity of glycosides. Close to maximum
effects of milrinone on cardiac output and pulmonary capillary pressure are seen at
milrinone plasma concentrations within the range of 150 ng/ml to 250 ng/ml.
Literature review identified clinical studies with patients treated for low cardiac
output syndrome following cardiac surgery, septic shock or pulmonary hypertension.
The usual dosages were a loading dose of 50 to 75 μg/kg administered over 30 to 60
minutes followed by an intravenous continuous infusion of 0.25 to 0.75 μg/kg/min for
a period up to 35 hours. In these studies, milrinone demonstrated an increase of
cardiac output, a decrease in cardiac filling pressure, a decrease in systemic and
pulmonary vascular resistance, with minimal changes in heart rate and in myocardial
oxygen consumption. Studies of a longer use of milrinone are not sufficient to
recommend an administration of milrinone during a period of more than 35 hours.
In vitro protein binding assays revealed that milrinone, depending on the assay
method used, is 70–91% protein-bound at therapeutically relevant plasma
concentrations. Six to twelve hours after a constant maintenance infusion of 0.50
micrograms/kg BW/min, steady-state plasma concentrations of milrinone are
approximately 200 ng/ml..
Following intravenous injections of 12.5 micrograms/kg BW to 125 micrograms/kg
BW in patients with heart failure, milrinone had a volume of distribution of 0.38 l/kg
BW, a mean terminal elimination half-life of 2.3 hours and a clearance of 0.13 l/kg
BW/h. Following intravenous infusions of 0.20 micrograms/kg BW/min to 0.7
micrograms/kg BW/min in patients with heart failure, the substance had a volume of
distribution of approximately 0.45 l/kg BW, the mean terminal elimination half-life
was 2.4 hours and clearance was 0.14 l/kg BW/h. These pharmacokinetic parameters
were not dose-dependent. Conversely, the area under the plasma concentration-time
curve after the injections was significantly dose-dependent. Via ultracentrifugation,
milrinone was shown to be up to 70% bound to human plasma proteins at plasma
concentrations between 70 and 400 nanograms/ml. Both clearance and half-life were
prolonged in patients with heart failure in relation to their degree of renal impairment
compared to healthy subjects. Data from patients with severe renal insufficiency
(creatinine clearance less than 30 ml/min) showed that the terminal elimination halflife is prolonged in cases of renal insufficiency.
Biotransformation and Elimination
In man, milrinone is mainly excreted in the urine. The main excretory products in
humans are milrinone (83%) and its O-glucuronide metabolite (12%). In healthy
subjects, excretion in the urine is rapid; approximately 60% is recovered in the urine
within the first two hours after administration and approximately 90% of the dose
within the first eight hours after administration. Mean renal clearance of milrinone IV
is approximately 0.3 l/min; this is indicative of active secretion.
Milrinone is cleared more rapidly in children than in adults, but infants have
significantly lower clearance than children, and preterm infants have even lower
clearance. As a consequence of this more rapid clearance compared to adults, steadystate plasma concentrations of milrinone were lower in children than in adults. In
paediatric population with normal renal function steady-state milrinone plasma
concentrations after 6 to 12 hours continuous infusion of 0.5 to 0.75 µg/kg/min were
about of 100 to 300 ng/ml.
Following intravenous infusion of 0.5 to 0.75 µg/kg/min to neonates, infants and
children after open heart surgery, milrinone has a volume of distribution ranging from
0.35 to 0.9 litres/kg with no significant difference across age groups. Following
intravenous infusion of 0.5 µg/kg/min to very preterm infants to prevent low systemic
outflow after birth, milrinone has a volume of distribution of about 0.5 litres/kg.
Several pharmacokinetic studies showed that, in paediatric population, clearance
increases with increasing age. Infants have significantly lower clearance than children
(3.4 to 3.8 ml/kg/min versus 5.9 to 6.7 ml/kg/min). In neonates milrinone clearance
was about 1.64 ml/kg/min and preterm infants have even lower clearance (0.64
Milrinone has a mean terminal half-life of 2 to 4 hours in infants and children and a
mean terminal elimination half-life of 10 hours in preterm infants.
It was concluded that the optimal dose of milrinone in paediatric patients in order to
obtain plasma levels above the threshold of pharmacodynamic efficacy appeared
higher than in adults, but that optimal dose in preterms in order to obtain plasma
levels above the threshold of pharmacodynamic efficacy appeared lower than in
Milrinone is cleared by renal excretion and has a volume of distribution that is
restricted to extracellular space which suggests that the fluid overload and
hemodynamic changes associated with patent ductus arteriosus may have an effect on
distribution and excretion of milrinone (see section 4.2, 4.4, 4.8, and 5.3).
Preclinical safety data
After oral administration, the LD50 for male mice is 137 mg/kg and for female mice
170 mg/kg, while the LD50 for male rats is 91 mg/kg and for female rats 153 mg/kg.
After intravenous administration of milrinone, focal epicardial and endocardial
haemorrhages and focal myocardial fibroses (particularly in the papillary muscle and
in the endocardial areas) occur in rabbits.
Subacute toxicity was examined in rats and dogs. In dogs, endocardial haemorrhages
and myocardial fibroses occurred in all treated groups after cumulative and fractioned
administration of milrinone in quantities just above the therapeutic dose.
Subchronic and chronic toxicity
Oral and intravenous application of milrinone to rats, dogs and monkeys lead in
therapeutic doses, or in doses just above the therapeutic dose, to myocardial
degenerations, fibroses and, particularly in the region of the papillary muscles of the
left ventricle, to subendocardial haemorrhages. Lesions of the coronary vessels,
characterised by a periarterial oedema and inflammation, were only observed in dogs.
In long-term trials, no tumour-producing potential was detected in rats and mice.
Endocardial haemorrhages and myocardial necroses and fibroses occurred in rats. At
the highest dosage, myocardial degenerations and fibroses were detected in mice. In
the stomachs of mice, necroses and ulcers were detected.
A detailed in vitro and in vivo test on mutagenicity produced negative results.
Milrinone, at oral doses of up to 40 times the usual human therapy dose, did not have
an effect on the fertility of male and female rats. Studies of the reproductive
toxicology in rats and rabbits did not produce any evidence of a teratogenic action at
doses of up to 10 times (oral) and 2.5 times (i.v.) of the usual human therapy dose.
In a study spanning 3 generations (P, F1, F2 generation) of rats treated orally with
milrinone, no effect on the development of the animals and their reproductive
capacity was detected in the mothers or the descendents, even at the highest dose (40
times the usual human therapy dose).
Embryonic/fetal dose in relation to the mother’s serum concentration:
A diaplacental transmission of milrinone to the fetus is documented in a study of
pregnant monkeys which had human therapy doses administered intravenously. The
ratio of maternal serum values to fetal serum levels was 4:1.
A preclinical study was performed to clarify the ductus-dilating effects of PDE 3
inhibitors in near-term rat pups and their differential effects in near-term and preterm
fetal rats. Postnatal ductus arteriosus dilatation by milrinone was studied with three
doses (10, 1 and 0.1mg/kg). The dilating effects of milrinone in the fetal ductus
constricted by indomethacin were studied by simultaneous administration of
milrinone (10, 1 and 0.1mg/kg) and indomethacin (10 mg/kg) to the mother rat at D21
(near-term) and D19 (preterm). This in vivo study has shown that milrinone induces
dose-dependent dilation of the fetal and the postnatal constricted ductus arteriosus.
Dilating effects were more potent with injection immediately after birth than at 1 hour
after birth. In addition, study showed that the premature ductus arteriosus is more
sensitive to milrinone than the mature ductus arteriosus (see section 4.2, 4.4, 4.8, and
List of excipients
Water for Injections
Sodium Hydroxide (for pH adjustment)
Furosemide or bumetanide should not be administered in intravenous lines containing
Milrinone 1 mg/ml Solution for injection or infusion since precipitation occurs on
admixture. Sodium Bicarbonate Intravenous infusion should not be used for dilution.
The medicinal product must not be mixed with other medicinal products except those
mentioned in section 6.6.
Unopened: 30 months
After dilution: A diluted solution of Milrinone 1 mg/ml Solution for injection or
infusion should be used within 24 hours.
From a microbiological point of view, unless the method of opening and dilution
precludes the risk of microbial contamination, the product should be used
immediately. If not used immediately, in-use storage times and conditions are the
responsibility of the user.
Special precautions for storage
Do not store above 25°C. Do not freeze.
Discard any unused product.
For storage after dilution of the medicinal product, see section 6.3.
Nature and contents of container
10 ml clear glass ampoule (type I), with a blister pack size of 5, 10 and 25 ampoules.
Not all pack sizes may be marketed.
Special precautions for disposal
Infusion solutions diluted as recommended with 0.45% saline, 0.9% saline or 5%
glucose should be freshly prepared before use. Parenteral drug products should be
examined visually and should not be used if particulate matter or discolouration are
Any unused product or waste material should be disposed of in accordance with local
MARKETING AUTHORISATION HOLDER
Claris Lifesciences UK Limited
Crewe Hall, Crewe, Cheshire CW16UL
MARKETING AUTHORISATION NUMBER(S)
DATE OF FIRST AUTHORISATION/RENEWAL OF THE
DATE OF REVISION OF THE TEXT
Source: Medicines and Healthcare Products Regulatory Agency
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