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Active substance(s): PHENYTOIN SODIUM

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Phenytoin Hikma 50 mg/ml
solution for injection
phenytoin sodium
Read all of this leaflet carefully before you start using this medicine because it
contains important information for you.
• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others. It may harm
them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side
effects not listed in this leaflet.


1.What Phenytoin Hikma is and what it is used for
2.What you need to know before you use Phenytoin Hikma
3.How to use Phenytoin Hikma
4.Possible side effects
5.How to store Phenytoin Hikma
6.Contents of the pack and other information

Phenytoin Hikma 50 mg/ml solution for injection contains phenytoin sodium. Phenytoin
sodium belongs to a group of medicines called antiepileptics. Antiepileptic medicines are
used for the prevention and treatment of seizures (fits). The medicine will be given to you by a
doctor and will be injected into a vein (intravenously).
Phenytoin Hikma is used to:
• Treat the following types of seizure:
– status epilepticus (a state of persistent seizure). A persistent seizure is when:
- you have a seizure that does not stop
- you have a number of seizures and remain unconscious throughout
• Prevent seizures happening during or after neurosurgery (surgery on the brain).
Phenytoin Hikma is not effective in absence status epilepticus (a special form of seizures) or
in the prevention or treatment of febrile convulsions.

A small number of people being treated with anti-epileptics such phenytoin have had
thoughts of harming or killing themselves. If at any
Do not use Phenytoin Hikma
• if you are allergic to phenytoin or any of the other ingredients of this medicine (listed in
section 6).
• if you are allergic (hypersensitive) to other medicines with a similar chemical structure to
phenytoin (e.g. hydantoins)
• if you have severe damage to the blood cells and bone marrow
• if you have grade II and grade III AV block (disorder of heart beat regulation)
• if you have a type of heart disorder that causes fainting and sometimes fits called StokesAdams syndrome.
• if you suffer from sinus bradycardia (slow heart rate of less than 50 beats per minutes),
sick sinus syndrome or sino-atrial block (disorders of heart beat regulation)
• if you have had a heart attack within the last three months
• if the output of your heart is poor (ask your doctor)
• subcutaneously or venous perivascular or intra-arterial due to the high pH of the
Warnings and precautions
A small number of people being treated with anti-epileptics such as phenytoin have
had thoughts of harming or killing themselves. If at any time you have these thoughts,
immediately contact your doctor.”
Phenytoin Hikma should not be given in
• heart failure (inability of heart to pump properly)
• impaired breathing function
• severe hypotension (systolic blood pressure less than 90 mm Hg)
• the following heart rhythm disturbances:
– grade I AV block
– atrial fibrillation
– atrial flutter
Phenytoin Hikma should be given with special precaution if you suffer from:
• impaired kidney function
• impaired liver function
your doctor will take blood and urine samples to monitor your liver and kidney function.
If you are diabetic you are more likely to get hyperglycaemia (high blood sugar).
Potentially life-threatening skin rashes (Stevens-Johnson syndrome, toxic epidermal
necrolysis) have been reported with the use of Phenytoin Hikma, appearing initially as reddish
target-like spots or circular patches often with central blisters on the trunk.
Additional signs to look for include ulcers in the mouth, throat, nose, genitals and
conjunctivitis (red and swollen eyes).
These potentially life-threatening skin rashes are often accompanied by flu-like symptoms.
The rash may progress to widespread blistering or peeling of the skin.
The highest risk for occurrence of serious skin reactions is within the first weeks of
vIf you have developed Stevens-Johnson syndrome or toxic epidermal necrolysis with the use
of Phenytoin Hikma, you must not be re-started on Phenytoin Hikma at any time.
Serious skin side effects can rarely occur during treatment with Phenytoin Hikma. This risk
may be associated with a variant in genes in a subject with Chinese or Thai origin. If you are
of such origin and have been tested previously carrying this genetic variant (HLA-B*1502),
discuss this with your doctor before taking Phenytoin Hikma.
If you develop a rash or these skin symptoms, stop taking Phenytoin Hikma, seek urgent
advice from a doctor and tell him that you are taking this medicine.
Important information regarding treatment
If you suffer from slow hydroxylation
Slow hydroxylation is an inherited disorder. It affects the way your body uses and reacts to
If you suffer from slow hydroxylation you should therefore take care. You may develop signs
of overdose even at moderate doses (see “What you must do if you are given too much
Phenytoin Hikma”). In this case your dose should be reduced. Your doctor will take a blood
sample to check that the levels of phenytoin are not too high.
If you switch to another form of medicine that contains phenytoin
Other medicines that contain phenytoin may not provide you with the same levels of
phenytoin as Phenytoin Hikma. If you change your phenytoin medicine, your doctor will
monitor you until your phenytoin levels even out. This may take up to 2 weeks.
If you suddenly stop taking Phenytoin Hikma
• you may suffer seizures more often
• you may develop status epilepticus (a state of persistent seizure).
To avoid these problems your doctor may:
• reduce your dose of Phenytoin Hikma slowly
• start the new antiepileptic medication at a low dose and gradually increase it
If you switch treatment to an oral form of phenytoin (e.g. tablets or syrup):
Your doctor will monitor your progress and take blood samples regularly.
If you are a child, your doctor will also monitor the function of your thyroid gland.
Your doctor will decide if any of the test results mean that you should change or stop
If you have low plasma protein levels (hypoproteinaemia) you are more likely to develop
undesirable effects on your nervous system.


Other medicines and Phenytoin Hikma
Please tell your doctor or pharmacist if you are taking or have recently taken any other
medicines, including medicines obtained without a prescription.
A number of medicines can increase or decrease the levels of phenytoin in the blood.
Phenytoin can alter the levels of other medicines in the blood. These effects are called
interactions. If your doctor thinks that you are having a drug interaction he will check your
phenytoin levels.
The following substances can increase your phenytoin levels:
• Alcohol (rapid consumption)
• Oral anticoagulants (blood-thinning medicines e.g. dicumarol)
• Benzodiazepines (tranquillisers e.g. chlorodiazepoxide, diazepam, trazodone)
• Anaesthetics (e.g. halothane)
• Other antiepileptic drugs (e.g. sulthiame, valproate, ethosuximide, mesuximide, felbamate)
• Non-steroidal antirheumatics (NSAIDs)(e.g. salicylate, azapropazone, phenylbutazone)
• Antibiotics (e.g. chloramphenicol, erythromycin, isoniazide, sulfonamide)
• Antimycotics (antifungal medicines e.g. amphotericin B, fluconazole, ketoconazole,
miconazole, itraconazole)
• Calcium channel inhibitors (heart medicines e.g. amiodarone, diltiazem, nifedipine)
• Hormones (e.g. oestrogen)
• Disulfiram (used to treat addiction to alcohol)
• Methylphenidate (used to treat attention deficit hyperactive disorder [ADHD])
• Cimetidine, omeprazole, ranitidine (used to treat stomach ulcers)
• Ticlopidine (used to prevent thrombosis)
• Viloxazine, fluoxetine (an antidepressant medicine)
• Para-amino salicylic acid (PAS), cycloserine (used to treat tuberculosis)
• Tricyclic antidepressant drugs (e.g. amitriptyline, clomipramine)
• Tolbutamide (used to treat diabetes)
• Other antiepileptic drugs (e.g. oxcarbazepine, eslicarbazepine acetate and in individual
patients topirmate
Substances that can decrease your phenytoin levels:
• Antibiotics (e.g. ciprofloxacin, rifampicin)
• Other antiepileptic drugs (e.g. carbamazepine, vigabatrine, phenobarbital, primidone)
• Reserpine (used to treat high blood pressure)
• Sucralfate (used to treat duodenal ulcers)
• Diazoxide (used to treat high blood pressure)
• Theophylline (used to treat breathing difficulties)
• Chronic alcohol abuse (persistent long-term alcohol abuse)
• Nelfinavir (used to treat viral infections caused by HIV (AIDS))
Substances that can increase or decrease your phenytoin levels:
• Antiepileptics (e.g. carbamazepine, sodium valproate, valproic acid, phenobarbital)
• Chlordiazepoxide (a sedative)
• Diazepam (a tranquilliser)
Valproic acid (an antiepileptic medicine): If you are given valproic acid in addition to phenytoin
or the dose of valproic acid is increased you may experience more side effects. In particular,
you are more likely to suffer brain damage (see section 4 “Possible side effects“).
Phenytoin can alter the concentration of the following medicines in your blood and
the effect of the medicine:
• Clozapine (used to treat schizophrenia)
• Corticosteroids (e.g. dexamethasone, prednisone, fludrocortisone)
• Oral anticoagulants (blood thinning medicines e.g. dicumarol)
• Doxycycline, tetracycline (antibiotics)
• Praziquantel (used to treat infestation with worms)
• Rifampicin (used to treat tuberculosis)
• Itraconazole (an antifungal medicine)
• Antiepileptics (e.g. lamotrigine, carbamazepine, valproate, felbamate, topiramate,
zonisamide or tiagabine and the active metabolite of oxcarbazepine (i.e. MHD) and
eslicarbazepine acetate (i.e. eslicarbazepine))
• Oestrogen (used in hormone replacement therapy [HRT])
• Alcuronium, pancuronium, vecuronium (muscle relaxants)
• Cyclosporine (used to prevent organ transplant rejection)
• Diazoxide (used to treat high blood pressure)
• Furosemide (a diuretic [water tablet] used to treat heart failure)
• Paroxetine, sertraline (antidepressants)
• Theophylline (used to treat breathing difficulties)
• Digitoxin (a heart medicine)
• Nicardipine, verapamil (used to treat high blood pressure)
• Nimodipine (used to prevent spasm of the blood vessels in the brain)
• Quinidine (a heart medicine)
• Tricyclic antidepressant drugs (e.g. amitriptyline, clomipramine)
• Methadone (used to treat heroin addiction)
• Chlorpropamide, glibenclamide (used to treat diabetes)
• Tolbutamide (used to treat diabetes)
• Vitamin D
• Teniposide (an anticancer medicine)
• Oral contraceptives: If you take the contraceptive pill its effect may be unreliable.
• Blood thinning medicines (anticoagulants): If you are taking such medicines you should
regularly check your blood clotting time (INR value).
• Methotrexate (an anticancer medicine): You may experience:
• a greater number of unwanted side effects of methotrexate treatment or
• worsening of side effects of methotrexate treatment
• Folic acid: Your phenytoin may not be so effective if you take folic acid at the same time.
Phenytoin Hikma, when administered concomitantly with paracetamol products may increase
the metabolism of paracetamol which can result in liver damage.
Pregnancy and Breast-feeding
You should note that the contraceptive pill may not work when you are taking Phenytoin
If you are planning to become pregnant or are already pregnant, you should only use
Phenytoin Hikma if your doctor tells you to, after a careful risk-benefit assessment.
If you are pregnant and treated with any antiepileptic drug it is more likely that your unborn
child will have an abnormality. Evidence suggests that it is 2 to 3 times more likely. Possible
abnormalities include:
• hare lip
• heart abnormalities
• underdeveloped nails or fingers, toes, face
• neural tube defects (the neural tube is the part of the body which develops into the nervous
• retarded growth
Therefore you should speak to your doctor immediately if you are planning to become
pregnant or are already pregnant. Your doctor will check whether treatment with Phenytoin
Hikma is necessary.
If it is urgent that you receive treatment with Phenytoin Hikma during pregnancy:
• You should not be given other antiepileptic medications if possible. Taking more epilepsy
medicines will increase the risk of abnormalities in your unborn child.
• During the first 3 months of pregnancy in particular, you should be given the lowest
effective dose. This is the lowest possible dose at which your seizures are well controlled.
Your doctor will decide this dose.
• Your condition and that of your unborn child will be monitored:
– Your serum levels of phenytoin will change during and after pregnancy. Your
doctor may monitor your serum levels of phenytoin to help make sure that you
get the right dose.
– You should be offered an ultrasound scan. Such a scan can show a detailed
picture of your unborn child. You should be told of any problems with the
condition of your unborn child.

Phenytoin Hikma 50 mg/ml solution for injection
Active substance: phenytoin sodium

The following information is intended for medical or healthcare professionals only:
Method of administration:
The solution for injection is for intravenous use only as absorption is delayed and
unreliable after intramuscular administration. Phenytoin Hikma should be injected slowly
directly into a large vein through a large-gauge needle or intravenous catheter.
Subcutaneous or venous injection should be avoided, as the alkaline phenytoin solution
for injection can cause tissue necrosis.
Handling and Preparation
The solution for injection must not be mixed with other solutions, as phenytoin can
crystallise out.

At a maximum daily dose of 17 mg/kg bodyweight, this is equivalent to
41 kg
690 mg
54 kg
920 mg
68 kg
1150 mg
81 kg
1380 mg
Children up to 12 years of age
On day 1 the maximum daily dose is 30 mg/kg bodyweight, on day 2 20 mg/kg
bodyweight, on day 3 10 mg/kg bodyweight. The maximum injection rate is 1 mg/kg
bodyweight per minute.

Before use, the ampoules should be checked for precipitation and discolouration.
The product should not be used if a precipitate or haziness develops in the solution in the
Phenytoin is suitable for use as long as it remains free of haziness and precipitate. A
precipitate might form if the product has been kept in a refrigerator or freezer. This
precipitate will dissolve if allowed to stand at room temperature. The product will then be
suitable for use.
Only a clear solution should be administered. A slight yellow discolouration has no effect
on the efficacy of this solution.

Day 1
At a maximum daily dose of 30 mg/kg bodyweight, this is equivalent to
8 kg
230 mg
15 kg
460 mg
23 kg
690 mg
31 kg
920 mg
38 kg
1150 mg
46 kg
1380 mg

For single use only. Any unused product should be discarded.

Day 2
At a maximum daily dose of 20 mg/kg bodyweight, this is equivalent to
12 kg
230 mg
23 kg
460 mg
35 kg
690 mg
46 kg
920 mg

Duration of administration is dependent on the underlying disease and the course of the
illness. If the medicine is well-tolerated, it can be used indefinitely.
The therapeutic range for plasma concentration is generally between 10 and 20
micrograms/ml phenytoin; concentrations over 25 micrograms/ml phenytoin may be in
the toxic range.
Status epilepticus and series of seizures
Continuous monitoring of ECG, blood pressure and neurological status and regular
determination of plasma phenytoin concentrations is essential. In addition, resuscitation
facilities should be readily available.
Adults and adolescents over 12 years of age
The initial dose is 1 ampoule of Phenytoin Hikma (equivalent to 230 mg phenytoin),
administered at a maximum rate of 0.5 ml/min (equivalent to 23 mg phenytoin per
minute). If the seizures do not stop after 20 to 30 minutes, the dose can be repeated.
If the seizures stop, a dose of 1 ampoule Phenytoin Hikma (equivalent to 230 mg
phenytoin) can be given every 1.5 to 6 hours up to a maximum daily dose of 17 mg/kg
bodyweight (or 6 ampoules - equivalent to 1380 mg phenytoin), to achieve rapid

Day 3
At a maximum daily dose of 10 mg/kg bodyweight, this is equivalent to
23 kg
230 mg
46 kg
460 mg
Prophylaxis of seizures
Adults and adolescents over 12 years of age receive 1 to 2 ampoules of Phenytoin Hikma
(equivalent to 230 to 460 mg phenytoin) daily at a maximum rate of injection of 0.5 ml/
min (equivalent to 23 mg phenytoin per minute).

Do not suddenly stop treatment with Phenytoin Hikma during pregnancy. Suddenly stopping
treatment can cause seizures. This can be harmful for you and your unborn child.

• Laboratory tests should be performed every six months, especially in children, owing to

Care of your new-born child
Your newborn child may develop bleeding disorders in the first 24 hours after birth. To
prevent this:
• Your doctor should give you a dose of vitamin K1 in the last week of pregnancy
• Your doctor should give your new-born child a dose of vitamin K1

• dyskinesia (diminished voluntary movements and the presence of involuntary movements),

possible impairment of thyroid function.

Prevention of folic acid deficiency
To prevent possible folic acid deficiency you should take folic acid during pregnancy. This
can be taken as tablets or as a food supplement. Your doctor will tell you how much to take.
When you take folic acid your phenytoin may not be so effective (see also “Using other
Small amounts of the active substance (phenytoin sodium) pass into human breast milk. It is
recommended that you do not breast-feed while receiving treatment with Phenytoin Hikma.
However, should you still wish to breast-feed, your baby should be monitored to make sure:
• it is gaining weight properly
• it does not have an increased need to sleep
Driving and using machines
Do not drive or use machines if your ability to drive and use machines is reduced.
Before driving or using machines seek your doctor’s advice.
Your ability to drive or operate machinery may be impaired:
• at the start of treatment with Phenytoin Hikma
• at high doses
• when this medicine is combined with drugs that affect your central nervous system
(especially alcohol)
Important information about some of the ingredients of Phenytoin Hikma
Phenytoin Hikma contains less than 23 mg sodium in each glass vial (ampoule). It is almost
Phenytoin Hikma contains propylene glycol which may cause alcohol-like symptoms.
This medicinal product contains 10 vol % ethanol (alcohol), i.e. up to 394 mg per dose,
equivalent to 10 ml beer, 4.17 ml wine per dose.
Harmful for those suffering from alcoholism.
To be taken into account in pregnant or breast-feeding women, children and high-risk groups
such as patients with liver disease, or epilepsy.

More detailed information on dosage, handling and preparation of Phenytoin
Hikma is given at the end of this package leaflet under the subheading ‘The
following information is intended for medical or healthcare professionals only’.
Phenytoin Hikma will be given to you by your doctor by slow injection into a vein. Your doctor
will decide on how much you need and when it is to be given. This will depend on your age
and weight and the condition for which you need to take Phenytoin Hikma.
When you are given Phenytoin Hikma your doctor will:
• continuously monitor your heart, blood pressure and nervous system
• regularly measure your phenytoin levels
Duration of therapy
Phenytoin Hikma can be used long-term.
Duration of therapy depends on:
• which illness you are being treated for
• how well you respond to treatment
• how well you tolerate the side-effects (see Section 4 “Possible side effects”).
During long-term treatment with Phenytoin Hikma your plasma levels will be monitored so
that you can be given the lowest effective dose. This will help to minimise side-effects.
Please speak to your doctor or pharmacist if you feel that the effect of Phenytoin Hikma is too
strong or too weak.
If you use more Phenytoin Hikma than you should:
If you are given too much Phenytoin Hikma you may experience the following: symptoms:
Early symptoms
• involuntary rapid eye movement (nystagmus)
• cerebellar ataxia (a disorder of movement coordination)
• dysarthria (impaired speech)
Other symptoms
• tremor (shaking)
• hyperreflexia (increased reflexes)
• somnolence (drowsiness)
• exhaustion
• lethargy (sluggishness)
• slurred speech
• diplopia (double vision)
• dizziness
• nausea (feeling sick)
• vomiting
• coma (loss of consciousness)
• your pupillary reflex (when the pupil of your eye gets smaller in response to light) may
• fall in blood pressure
• effects on breathing. These can be fatal.
• heart failure. This can be fatal.
• irreversible brain damage
If you experience any of these symptoms, you should tell your doctor immediately. Your doctor
will take steps to remove the excess phenytoin from your system. Your heart and breathing
will be monitored and your symptoms will be treated.

chorea (involuntary movement disorder), dystonia (twisting and repetitive movements or
abnormal postures), tremor and asterixis (flapping tremor). asystole (flatline), conduction
blockade and suppression of the ventricular escape rhythm in patients with total AV block,
especially when phenytoin is administered intravenouslly. Proarrhythmic effects in the
form of changes or increases in cardiac arrythmias can occur which can lead to severe
impairment of cardiac activity or even cardiac arrest. With intravenous administration in
particular, decreased blood pressure, deterioration in existing heart and respiratory failure
can occur. In isolated cases ventricular fibrillation has been triggered. Atrial fibrillation and
flutter is not cured by phenytoin. However, as AV node refractory time can be shortened,
acceleration in ventricular rate is possible.
liver function disorders, possibly with involvement of other organs, if developed, it is
recommended to discontinue phenytoin treatment. The symptoms may also gradually
subside if the dose is reduced. Therefore, when phenytoin is taken long-term, liver enzyme
activity should be checked at regular intervals (several weeks).
allergic rashes (exanthema); severe allergic reactions e.g. skin inflammation with exfoliative
softening of the bones caused by defective bone mineralization (osteomalacia), may
develop in susceptible patients or patients with a calcium metabolism disorder (increased
alkaline phosphatase). This normally responds well to administration of vitamin D. Alkaline
phosphatase should therefore be checked regularly.
fever (together with rash). Local irritation, inflammation and tenderness have been reported.
Necrosis and sloughing have been reported after subcutaneous or perivascular injection,
which are not recommended administration routes. Soft tissue irritation and inflammation
have occurred at the site of injection with and without extravasation of phenytoin given

Very rare side effects (may affect up to 1 in 10,000 people):
• systemic lupus erythematosus, periarteritis nodosa (vasculitis of medium and small-sized
arteries) and immunoglobulin abnormalities may occur.
• excessive growth of gum tissue (gingival hyperplasia), skin changes e.g. and hair growth
(hypertrichosis, hirsutism), have been reported. Dupuytren’s contracture, Stevens-Johnson
and Lyell’s syndrome, have also been reported. Severe cutaneous adverse reactions
(SCARs): Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) have been
reported (see section 4.4).
• muscle weakness (myasthenic syndrome) which subside after phenytoin is withdrawn.
Side effects which frequency is not known (Frequency cannot be estimated from the
available data):
• Purple Glove Syndrome (skin disease in which the extremities become swollen, discoloured
and painful) has been reported. Tell your doctor immediately if you experience skin
discolouration, swelling and pain where the injection was given which then starts to spread
down your arm to your hands and fingers. This may mean you have of a condition known
as “purple glove syndrome”. In most cases this will improve on its own but in some cases it
can be serious and require urgent medical treatment.
Side effects of long-term therapy
Frequency not known: (cannot be estimated from the available data)
• sensory peripheral polyneuropathy (disturbed nerve function) and tonic seizures
• irreversible cerebellar atrophy (permanent wasting away of the brain)
If you take phenytoin long-term (especially when taken by mouth) you may develop signs
of brain damage (encephalopathy). This is especially likely when taken together with other
antiepileptic medicines, especially valproic acid. Signs of brain damage include:
Frequency not known: (cannot be estimated from the available data)
• more frequent seizures
• loss of drive (stupor)
• weak muscles (muscular hypotension)
• choreatic dyskinesia (a movement disorder)
• severe general changes on your brain scan (EEG)
• There have been reports of bone disorders including osteopenia and osteoporosis (thinning
of the bone) and fractures. Check with your doctor or pharmacist if you are on long-term
antiepileptic medication, have a history of osteoporosis, or take steroids.
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side
effects not listed in this leaflet.

Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP.. The
expiry date refers to the last day of that month.
This medicinal product does not require any special storage conditions.
After first opening: Phenytoin Hikma should be used immediately.
If the solution in the ampoule is cloudy or contains solids, the ampoule should not be used.
Do not throw away any medicines via wastewater.. Ask your pharmacist how to throw away
medicines you no longer use. These measures will help protect the environment.

What Phenytoin Hikma contains
The active substance is phenytoin sodium.
Each ml of solution contains 50 mg phenytoin sodium (equivalent to 46 mg phenytoin).
Each 5 ml-ampoule of solution for injection contains 250 mg phenytoin sodium (equivalent to
230 mg phenytoin).
The other ingredients are:
• propylene glycol
• ethanol
• sodium hydroxide
• water for injection


What Phenytoin Hikma looks like and contents of the pack
Phenytoin Hikma is supplied in clear glass vials called ampoules.

Like all medicines, Phenytoin Hikma can cause side effects, although not everybody gets

Phenytoin Hikma is a clear solution.

Very common side effects (may affect more than 1 in 10 people):
• nystagmus (rapid eye movement), movement coordination disorders (ataxia), paresthesia
(“pins and needles” feeling), mental confusion, dizziness, vertigo, insomnia, headache,
increasing irritability, high-frequency tremor at rest, bulbar speech disorders, exhaustion,
memorising disturbances and intellectual capacity disorders.
• double vision (diplopia)
Common side effects (may affect up to 1 in 10 people):
• apathy and sedation, perception disorders and clouding of consciousness, or even coma,
have been reported for long-term treated patients
• transient symptoms such as dizziness, vomiting and dry mouth can develop if intravenous
administration is too fast, which generally subside within 60 minutes unless the patient
has received a medication containing phenytoin before. Loss of appetite, nausea, vomiting,
weight loss, constipation, have also been reported for long-term treated patients.
• morbiliform rash (measles-like)
Uncommon side effects (may affect up to 1 in 100 people):
• polyneuropathy may develop in the context of long-term therapy (with risk of occurrence of
irreversible cerebellar atrophy).
• severe general changes on the ECG have been reported for patients undergoing long-term
treatment with phenytoin.
Rare side effects (may affect up to 1 in 1,000 people):
• changes in blood count, e.g. leukopenia (decrease number of white blood cells),
megaloblastic anaemia (formation of very large red blood cells), porphyria (disorders of
certain enzymes that normally participate in the production of porphyrins and heme) may
occur, if they do develop, it is recommended that phenytoin is withdrawn. The symptoms
may also gradually subside if the dose is reduced.
• anaphylaxis and anaphylaxis-type reactions and have been reported and may in rare cases
be fatal (the syndrome may include but is not limited to, symptoms such as arthralgias,
eosinophilia, fever, liver dysfunction, lymphadenopathy or rash)

Pack size: Phenytoin Hikma is available in packs of 5 or 50 ampoules.
1 ampoule contains 5 ml solution for injection.
Marketing Authorisation Holder and Manufacturer
Hikma Farmacêutica (Portugal), S.A.
Estrada do Rio da Mó n.º 8, 8A e 8B – Fervença
2705-906 Terrugem SNT, Portugal
Distributed by:
Consilient Health (UK) Ltd.
No. 1 Church Road, Richmond upon Thames, Surrey, TW9 2QE
This medicinal product is authorized in the Member States of the EEA under the
following names:
Phenytoin Hikma 50 mg/ml Injektionslösung
Phenytoin Hikma 50 mg/ml Soluzione iniettabile
Phenytoin Hikma 50 mg/ml Roztwór do wstrzykiwań
Fenitoina Hikma 50 mg/ml Solução injectável
Phenytoin Hikma 50 mg/ml Soluţie injectabilă
United Kingdom: Phenytoin Hikma 50 mg/ml Solution for injection
This leaflet was last approved in April 2016


Children up to 12 years of age receive 5 to 6 mg/kg bodyweight. Rate of injection is
reduced according to the weight/age of the child.
At a daily dose of 5 mg/kg bodyweight, this is equivalent to
9 kg
46 mg
18 kg
92 mg
28 kg
138 mg
37 kg
184 mg
46 kg
230 mg
At a daily dose of 6 mg/kg bodyweight, this is equivalent to
8 kg
46 mg
15 kg
92 mg
23 kg
138 mg
31 kg
184 mg
38 kg
230 mg
46 kg
276 mg
When Phenytoin Hikma is taken long-term, Phenytoin Hikma plasma levels must be
monitored and blood count and liver enzyme activity should be checked at regular
intervals (several weeks). A blood count showing moderate, stable leukopenia or an
isolated increase in gamma-GT should not normally necessitate withdrawal of treatment.
Osteomalacia (soft bones) may develop in susceptible patients or patients with a calcium
metabolism disorder (increased alkaline phosphatase). This normally responds well to
administration of vitamin D. Alkaline phosphatase should therefore be checked regularly.
Additionally in children, thyroid function should be monitored.
Switching preparations
Due to the relatively narrow therapeutic range and the varying bioavailability of the
numerous pharmaceutical preparations, when changing from one preparation to another
containing phenytoin, the phenytoin-plasma concentrations must be monitored closely. If
the dose is kept the same, steady state can be expected after 5 to 14 days.
Therefore the dose (if possible) should be reduced slowly and the new antiepileptic
medicine started at a low dose and gradually increased. Abrupt withdrawal of Phenytoin
Hikma may increase seizure frequency or lead to status epilepticus.

Additional information on special populations
Patients with renal/hepatic impairment:
There is no reference for dosage adjustment for this special group; however, caution
should be taken in patients with renal and hepatic disease (see section 4.4). Impaired
renal and hepatic functions require careful monitoring.
Elderly (over 65 years):
As for adults; however, complications may occur more readily in elderly patients.
In neonates it has been shown that absorption of phenytoin is unreliable after oral
administration. Phenytoin should be injected slowly intravenously at a rate of 1-3 mg/kg/
min at dose of 15-20 mg/kg. This will usually produce serum concentrations of phenytoin
within the generally accepted therapeutic range of 10-20 mg/l.
Infants and children:
As for adults. Children tend to metabolise phenytoin more rapidly than adults. This should
be considered when determining dosage regimens; monitoring serum levels is therefore
particularly beneficial in such cases.
Therapy of overdosage
Symptoms of an overdose
Signs of overdose can develop in individuals who have different phenytoin plasma levels.
Early symptoms include involuntary, rapid eye movement, cerebellar ataxia and dysarthria.
Additional symptoms may include: tremor, hyperreflexia, somnolence , exhaustion,
lethargy, slurred speech, diplopia , dizziness, nausea, vomiting. The patient may fall into a
coma, the pupillary reflex may disappear, and blood pressure fall. Death can result e.g.
from central respiratory depression or circulatory failure. The mean lethal (acute) dose is
estimated to be 2-5 g phenytoin in adults. The lethal dose for paediatric patients is
unknown. Overdose can lead to irreversible degenerative cerebellar changes.
Treatment of intoxication
Initial treatment must include gastric lavage, administration of activated charcoal and
monitoring on intensive care. Haemodialysis, forced diuresis and peritoneal dialysis are
less effective. Experience on the efficacy of haematogenic charcoal perfusion, total
plasma substitution and transfusion is inadequate. For this reason, intensive internal
treatment without special detoxification procedures should be performed, but phenytoin
plasma levels should be checked.

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