Ciprofloxacin Injection USP 200 mg/10Oml

 

• 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. See section 4.

What this leaflet contains

1. What Sodium oxybate oral solution is and what it is used for
2. What you need to know before you take Sodium oxybate oral solution
3. How to take Sodium oxybate oral solution
4. Possible side effects
5. How to store Sodium oxybate oral solution
6. Contents of the pack and other information

The name of this medicinal product is Sodium oxybate 500 mg/ml oral solution, referred to as Sodium oxybate oral solution in this leaflet.
Sodium oxybate oral solution contains the active substance sodium oxybate. Sodium oxybate works by consolidating night-time sleep, though its exact mechanism of action is unknown.

Sodium oxybate oral solution is used to treat narcolepsy with cataplexy in adults, adolescents and children from 7 years of age.
Narcolepsy is a sleep disorder that may include attacks of sleep during normal waking hours, as well as cataplexy, sleep paralysis, hallucinations and poor sleep. Cataplexy is the onset of sudden muscle weakness or paralysis without losing consciousness, in response to a sudden emotional reaction such as anger, fear, joy, laughter or surprise.

• if you are allergic to sodium oxybate or any of the other ingredients of this medicine (listed in section 6).
• if you have succinic semialdehyde dehydrogenase deficiency (a rare metabolic disorder).
• if you suffer from major depression.
• if you are being treated with opioid or barbiturate medicines.
• Talk to your doctor or pharmacist before taking Sodium oxybate oral solution:
• if you have breathing or lung problems (and especially if you are obese), because sodium oxybate has the potential to cause difficulty in breathing.
• if you have or have previously had depressive illness, suicidal thoughts, anxiety, psychosis (a mental disorder that may involve hallucinations, incoherent speech, or disorganized and agitated behavior) or bipolar disorder.
• if you have heart failure, hypertension (high blood pressure), liver or kidney problems as your dose may need to be adjusted.
• if you have previously abused drugs
• if you suffer from epilepsy as the use of sodium oxybate is not recommended in this condition
• if you have porphyria (an uncommon metabolic disorder)
• If any of these apply to you, tell your doctor before you take Sodium oxybate oral solution.

While you are taking Sodium oxybate oral solution, if you experience bed wetting and incontinence (both urine and faeces), confusion, hallucinations, episodes of sleepwalking or abnormal thinking you should tell your doctor straight away. Whilst these effects are uncommon, if they do occur, they are usually mild-to-moderate in nature.

If you are elderly, your doctor will monitor your condition carefully to check whether sodium oxybate is having the desired effects.

Sodium oxybate has a well-known abuse potential. Cases of dependency have occurred after the illicit use of sodium oxybate.

Your doctor will ask if you have ever abused any drugs before you start taking Sodium oxybate oral solution and whilst you are using the medicine.

Sodium oxybate oral solution can be taken by adolescents and children from 7 years of age when they are over 15 kg in weight.

Sodium oxybate oral solution cannot be taken by children below 7 years of age or below 15 kg in weight.

If you are a child or adolescent, your doctor will monitor your body weight regularly.
Whilst the doctor is adjusting the dose which may take a number of weeks, parent/caregivers should carefully monitor the child's breath during the first 2 hours after sodium oxybate intake to assess if there is any abnormality in breathing, for example stoppage of breathing for short periods while sleeping, noisy breathing and bluish colour of the lips and face. If abnormality in breathing is observed medical support should be sought and the doctor should be informed as soon as possible. If any abnormality is noted after the first dose, the second dose should not be administered. If no abnormality is noted the second dose can be administered. The second dose should not be given earlier than 2½ hours or later than 4 hours after the first dose.

If you have had or are having upsetting feelings particularly if you are feeling very sad or have lost interest in life it is important that you tell the doctor or caregiver.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

In particular Sodium oxybate oral solution should not be taken together with sleep inducing medicines and medicines that reduce central nervous system activity (the central nervous system is the part of the body related to the brain and spinal cord).
Also tell your doctor or pharmacist if you are taking any of the following types of medicines:

• medicines that increase central nervous system activity
• antidepressants
• medicines that may be processed in a similar way by the body (e.g., valproate, phenytoin or ethosuximide which are used for the treatment of fits)
• topiramate (used for treatment of epilepsy)

If you are taking valproate, your daily dose of sodium oxybate will need to be adjusted (see section 3) as it may lead to interactions with valproate.

You must not drink alcohol while taking Sodium oxybate oral solution, as its effects can be increased.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.

There have been very few women who have taken sodium oxybate sometime during their pregnancy and a few of them had spontaneous abortions. The risk of taking sodium oxybate during pregnancy is unknown, and, therefore, the use of sodium oxybate in pregnant women or women trying to become pregnant is not recommended.
Patients taking sodium oxybate should not breast-feed since it is known that sodium oxybate passes into breast milk.

Changes in sleep patterns have been observed in breastfed infants from exposed mothers.

Sodium oxybate oral solution will affect you if you drive or operate tools or machines.

Do not drive a car, operate heavy machinery, or perform any activity that is dangerous or that requires mental alertness for at least 6 hours after taking Sodium oxybate oral solution. When you first start taking Sodium oxybate oral solution, until you know whether it makes you sleepy the next day, use extreme care while driving a car, operating heavy machinery or doing anything else that could be dangerous or needs you to be fully mentally alert.

For pediatric patients, physicians, parents or caregivers are advised that the waiting time for performing activities that require mental alertness, motor co-ordination or any activities that may have a physical risk may have to be longer than 6 hours, depending on individual sensitivity.

You need to monitor the amount of salt you take as Sodium oxybate oral solution contains sodium which may affect you if you have had high blood pressure, heart or kidney problems in the past.

The maximum recommended daily dose of this medicinal product for an adult contains 1.68 g sodium (found in table salt). This is equivalent to 84.2% of the adult recommended maximum daily dietary intake for sodium.

For every 2.25 g dose of sodium oxybate, this medicine contains 420.8 mg of sodium.
Talk to your pharmacist or doctor if you need Sodium oxybate oral solution on a nightly basis for a prolonged period of time, especially if you have been advised to have a low salt diet.

This medicine contains 0.23 mg benzalkonium chloride per 2.25 g sodium oxybate dose.
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

• For adults the recommended starting dose is 4.5 g each night, given as two separate doses of 2.25 g.
• Your doctor may gradually increase your dose up to a maximum of 9 g each night given as two separate doses of 4.5 g.
• Take Sodium oxybate oral solution orally two times each night:
• Take the first dose upon getting into bed and the second dose 2½ to 4 hours later. You may need to set an alarm clock to make sure you wake up to take the second dose.
• Food decreases the amount of sodium oxybate that is absorbed by your body. Therefore, it is best to take Sodium oxybate oral solution at set times 2 to 3 hours after a meal.
• Prepare both doses before bedtime.
• Take doses within 24 hours after preparation.
• If you are taking valproate together with Sodium oxybate oral solution, the dose of sodium oxybate will be adapted by your doctor.
• For those aged 7 years and over who weigh 15 kg or more, a doctor will work out the right dose based on your body weight.
• Your doctor will work out the right dose for you. Do not exceed the dose prescribed for you.
• If you are taking valproate together with Sodium oxybate oral solution, the dose of sodium oxybate will be adapted by your doctor.
• If you have kidney problems, you should consider a dietary recommendation to reduce sodium (salt) intake.
• If you have liver problems, the starting dose should be halved. Your doctor may gradually increase your dose.

The following instructions explain how to prepare Sodium oxybate oral solution. Please read the instructions carefully and follow them step by step. Do not allow children to prepare this medicine.

To help you, the Sodium oxybate oral solution carton contains 1 bottle of medicine, a measuring syringe and bottle-adaptor, and two dosing cups with child-resistant caps.

Step 1

• Remove the bottle cap by pushing down while turning the cap anticlockwise (to the left) (figure 1).

• After removing the cap, set the bottle upright on a table top.

• While holding the bottle in its upright position, insert the press-in bottle adaptor into the neck of the bottle. This needs only to be done the first time that the bottle is opened. The adaptor can then be left in the bottle for all subsequent uses.

Step 2

• Take the measuring syringe and insert the tip of the syringe into the center opening of the bottle adaptor opening and press down firmly (figure 2).

• Turn the bottle upside down (figure 3)

• Fill the measuring syringe with a small amount of solution by pulling the piston down, then push the piston upward in order to remove any possible bubbles. Finally, pull the piston down to the graduation mark corresponding to the quantity in grams (g) prescribed by your doctor (figure 4).

Step 3

• Turn the bottle the right way up.

• Remove the measuring syringe from the adaptor.

• Remove the cap from the first dosing cup by pressing down on the child resistant locking tab and turning the cap anticlockwise (to the left).

• Empty the medicine from the syringe into one of the dosing cups provided by pushing on the plunger (figure 6). Repeat this step for the second dosing cup.

• Then add about 60 ml of water to each dosing cup (60 ml is about 4 tablespoons).

Step 4

• Place the caps provided on the dosing cups and turn each cap clockwise (to the right) until it clicks and locks into its child-resistant position (figure 7).

• Rinse out the syringe with water.

• Just before going to sleep:

• Adult patients should place the second dose near their bed.

• The parent or caregiver of an adolescent or child should not leave the second dose near the child's bed or within easy reach of the child.

• You may need to set an alarm, so you wake up to take your second dose no earlier than 2½ hours and no later than 4 hours after your first dose.

Then:

• Remove the cap from the first dosing cup by pressing down on the child resistant locking tab and turning the cap anticlockwise (to the left).

• Drink all of the first dose while sitting in bed, recap the cup, and then lie down right away.

• When you wake up 2½ to 4 hours later, remove the cap from the second dosing cup. While sitting in bed, drink all of the second dose right before lying down to continue sleeping. Recap the second cup.

If you have the impression that the effect of Sodium oxybate oral solution is too strong or too weak, talk to your doctor or pharmacist.

Symptoms of sodium oxybate overdose may include agitation, confusion, impaired movement, impaired breathing, blurred vision, profuse sweating, headache, vomiting, decreased consciousness leading to coma and seizures, excessive thirst, muscle cramps and weakness. If you take more Sodium oxybate oral solution than you were told to take, or take it by accident, get emergency medical help right away. You should take the labelled medicine bottle with you, even if it is empty.

If you forget to take the first dose, take it as soon as you remember and then continue as before. If you miss the second dose, skip that dose and do not take Sodium oxybate oral solution again until the next night. Do not take a double dose to make up for a forgotten dose.

You should continue to take Sodium oxybate oral solution for as long as instructed by your doctor. You may find that your cataplexy attacks return if your medicine is stopped and you may experience insomnia, headache, anxiety, dizziness, sleeping problems, sleepiness, hallucination and abnormal thinking.

If you stop taking Sodium oxybate oral solution for more than 14 consecutive days, you should consult your doctor as you should restart taking Sodium oxybate oral solution at a reduced dose.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

Like all medicines, this medicine can cause side effects, although not everybody gets them. These are usually mild to moderate.
Adults - most common side effects observed in clinical studies (occurring in 10% to 20% of patients):

• dizziness

• nausea

• headache

If you experience any of these side effects, tell your doctor straight away.
Children and adolescents - most common side effects observed in a clinical study:

• bed wetting (18.3%)

• nausea (12.5%)

• vomiting (8.7%)

• weight decrease (8.7%)

• decreased appetite (6.7%)

• headache (5.8%)

• dizziness (5.8%)

• suicidal thoughts (1%)

• feeling mentally unwell (loss of contact with reality) (1%)

If you experience any of these side effects, tell your doctor straight away.
The side effects in adults and children are the same. If you experience any of the side effects listed below, tell your doctor straight away:
Very common (may affect more than 1 in 10 people)

• nausea

• dizziness

• headache

Common (may affect up to 1 in 10 people)

• sleeping problems including insomnia, abnormal dreams, sleep paralysis, sleepiness, nightmares, sleepwalking, bed wetting, excessive daytime sleepiness, difficulty in falling asleep in the middle of the night

• feeling drunk, trembling, confusion/ disorientation, blurred vision, balance disorder, fall, feeling of "spinning" (vertigo)

• feeling the heartbeat, increased blood pressure, shortness of breath

• vomiting, stomach pains, diarrhea

• anorexia, decreased appetite, weight loss.

• weakness, tiredness, sedation

• sweating

• depression

• muscle cramps, swelling.

• joint pain, back pain

• disturbance in attention, disturbed sensitivity particularly to touch, abnormal touch sensation, abnormal taste.

• anxiety, nervousness

• urinary incontinence

• snoring, congestion of the nose

• rash

• inflammation of the sinuses, inflammation of nose and throat

Uncommon (may affect up to 1 in 100 people)

• psychosis (a mental disorder that may involve hallucinations, incoherent speech, or disorganized and agitated behavior)

• paranoia, abnormal thinking, hallucination, agitation, suicide attempt

• difficulty in falling asleep, restless legs.

• forgetfulness

• myoclonus (involuntary contractions of muscles)

• involuntary passage of faeces

• hypersensitivity

Not known (cannot be estimated from the available data):

• convulsion

• decreased breathing depth or rate, short cessation of breathing during sleep.

• hives

• suicidal thoughts, delusion, thoughts of committing violent acts (including harming others)

• irritability, aggression

• euphoric mood

• panic attack

• mania / bipolar disorder

• dry mouth, dehydration

• swelling face (angioedema)

• bruxism (teeth grinding and jaw clenching)

• pollakiuria / micturition urgency (increased need to urinate)

• tinnitus (noise in the ears such as ringing or buzzing)

• sleep-related eating disorder

• increased appetite

• loss of consciousness

• dyskinesia (e.g. abnormal, uncontrolled movements of the limbs)

• dandruff

• increased sexual desire.

• nocturia (excessive urination at night)

• choking sensation

If you experience any of the side effects listed above, tell your doctor straight away.
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme, Website: www.mhra.gov.uk/yellowcard, or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects, you can help provide more information on the safety of this medicine.

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date stated on the carton box and bottle after ‘EXP’. The expiry date refers to the last day of that month.

After dilution in the dosing cups, the preparation should be used within 24 hours.
Once you open a bottle of Sodium oxybate oral solution, any contents that you have not used within 7 weeks of opening should be disposed of.

This medicine does not require any special storage conditions.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

• The active substance is sodium oxybate. Each ml contains 500 mg of sodium oxybate.

• The other ingredients are benzalkonium chloride, malic acid, sodium hydroxide, purified water.

Sodium oxybate oral solution is supplied in a 200 ml amber glass bottle containing 180 ml of oral solution and closed with a polypropylene/polyethylene child-resistant cap. Each pack contains one glass bottle, a LDPE press-in-bottle-adaptor (PIBA) and polypropylene/polyethylene measuring syringe, and two glass dosing cups with polypropylene/polyethylene child-resistant caps.
The oral solution is a clear, colorless to slightly yellow solution.
Unit 12 Farnborough Business Centre
Eelmoor Road Farnborough Hampshire GU14 7XA United Kingdom Dornbergsweg 3538855 Wernigerode Germany or Elisabeth-Selbert-Strade 23 40724 Langenfeld Germany.
This leaflet was last revised in April 2022.