$280.00 – $5,750.00
– Pethidine 100mg/2ml
120 Amps cost $280
250 Amps cost $500
500 Amps cost $850
1000 Amps cost $1500
2000 Amps cost $2500
5000 Amps cost $5750
1. Name of the medicinal product
Pethidine 50mg/ml & 100mg/2ml Solution for Injection
2. Qualitative and quantitative composition
Pethidine Hydrochloride 5% w/v
(50mg in 1ml and 100mg in 2ml total volume)
For the full list of excipients, see section 6.1
3. Pharmaceutical form
Solution for Injection
A clear colorless, particle-free solution
4. Clinical particulars
4.1 Therapeutic indications
Relief of moderate to severe pain.
Enhancement of analgesia
4.2 Posology and method of administration
For moderate or severe pain.
A normal single dose (usually not to be repeated more often than 4 hourly)
By intramuscular or subcutaneous injection
By slow intravenous injection
25 – 100 mg.
25 – 50 mg.
For obstetric analgesia.
By intramuscular or subcutaneous injection repeated 1 – 3 hours later. 50 – 100 mg.
Maximum of 400mg in 24 hours.
As a premedication.
By intramuscular injection one hour prior to the operation. 50 – 100mg
For the enhancement of analgesia.
By slow intravenous injection. 10 – 25mg as required.
Elderly or debilitated patients.
Initial doses should not exceed 25mg as this group of patients may be especially sensitive to the central depressant effect of the drug.
For moderate or severe pain.
By intramuscular injection. 0.5 – 2 mg per Kg of body weight.
As a premedication.
By intramuscular injection one hour prior to the operation. 1 – 2 mg per kg of body weight.
Method of administration
Intramuscular, intravenous or subcutaneous injection
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1
Severe respiratory depression, severe obstructive airways disease or acute asthma.
It should not be administered to patients with severe renal impairment or severe hepatic impairment.
Should be avoided in patients with acute alcoholism, delirium tremens raised intracranial pressure or in those with convulsive states such as status epilepticus.
It should not be administered to patients receiving monoamine oxidase inhibitors ( including moclobemide, and the monoamine B inhibitors selegiline and rasagiline) or within two weeks of their withdrawal.
Pethidine should not be administered to patients receiving ritonavir.
Use of pethidine should be avoided in patients with supraventricular tachycardia.
Use of pethidine in patients with phaeochromocytoma may result in hypertensive crisis.
Use of pethidine should be avoided in patients with diabetic acidosis where there is danger of coma.
In comatose patients
In patients with a risk of paralytic ileus
In patients with head injuries.
4.4 Special warnings and precautions for use
Pethidine is controlled under the Misuse of Drugs Act 1971 (Schedule 2).
Repeated use may result in dependence of the morphine type.
Pethidine should be used with caution in patients with acute or chronic airflow obstruction including asthma.
Pethidine should be used with caution or in reduced doses in patients with myasthenia gravis.
Pethidine should only be given with caution and in reduced doses to neonates, premature infants, patients who are elderly or debilitated or those with impaired hepatic or renal function. Renal impairment may result in accumulation of the potentially toxic metabolite norpethidine, particularly with repeat dosing All of these patient groups may experience increased or prolonged effects of the product.
Pethidine should be used with caution in patients with shock, hypothyroidism, Adreno-corticol insufficiency and a history of convulsive disorders.
Although less spasmogenic than morphine, pethidine may precipitate spasm of the ureter or Sphincter of Oddi. Subsequently, it should be used with caution in patients with prostatic hypertrophy and biliary tract disorders including those with pain secondary to gallbladder pathology.
Pethidine should be used with caution in patients with existing hypotension as it may reduce the blood pressure further.
In addition, it should be avoided in patients with severe inflammatory bowel disease due to its effects on the gastrointestinal tract where it may precipitate toxic megacolon.
The risk from the concomitant use of sedative medicines such as benzodiazepines or related drugs:
Concomitant use of methadone and sedative medicines such as benzodiazepines or related drugs may result in sedation, respiratory depression, coma, and death. Because of these risks, concomitant prescribing with these sedative medicines should be reserved for patients for whom alternative treatment options are not possible. If a decision is made to prescribe methadone concomitantly with sedative medicines, the lowest effective dose should be used, and the duration of treatment should be as short as possible.
The patients should be followed closely for signs and symptoms of respiratory depression and sedation. In this respect, it is strongly recommended to inform patients and their caregivers to be aware of these symptoms (see section 4.5).
4.5 Interaction with other medicinal products and other forms of interaction
Monoamine Oxidase Inhibitors
The concurrent use of MAOIs (including moclobemide) is contraindicated (see section 4.3) as they may result in CNS excitation or depression.
Pethidine should not be administered to patients receiving monoamine oxidase inhibitors or moclobemide or within two weeks of their withdrawal (see Section 4.3).
CNS depressants such as alcohol, hypnotics, anxiolytics and sedatives, barbiturates and tricyclic antidepressants may increase the general depressant effects of pethidine and should, therefore, be used with caution.
Additive effects on CNS depression, respiratory depression and hypotension can occur with concomitant use of opioid agonist analgesics.
Concomitant use of MAO-B inhibitors such as selegiline or rasagiline is contraindicated (see section 4.3) as this may lead to hyperpyrexia and CNS toxicity.
Rasagiline should not be given with pethidine as there is a risk of CNS toxicity, its use should be avoided for two weeks after taking rasagiline.
Administration of phenytoin may cause an increase in hepatic metabolism of pethidine and subsequently increased levels of norpethidine (a toxic metabolite).
Concomitant use of phenothiazines and pethidine can induce severe hypotension.
Plasma concentrations of pethidine may be decreased by concomitant administration of ritonavir, however levels of norpethidine (a toxic metabolite) may rise. Concomitant administration of ritonavir and pethidine should be avoided (see section 4.3).
Histamine H2 antagonists
Cimetidine can reduce the metabolism of pethidine resulting in increased plasma concentration.
Effects of pethidine on other drugs
Pethidine may have an effect on the activities of other drugs, for example, domperidone, as a consequence of reduced gastrointestinal motility.
The plasma levels of ciprofloxacin may be reduced in the presence of opiate premeditates.
Plasma levels of mexiletine may also be reduced in the presence of opioid analgesics.
Possible increased serotonergic effects when pethidine is given with SSRI’s.
Sedative medicines such as benzodiazepines or related drugs:
The concomitant use of opioids with sedative medicines such as benzodiazepines or related drugs increases the risk of sedation, respiratory depression, coma, and death because of additive CNS depressant effect. The dose and duration of concomitant use should be limited (see section 4.4).
4.6 Fertility, pregnancy, and lactation
There is inadequate evidence of safety in human pregnancy, but the drug has been in widely used for many years without apparent ill consequence. Animal studies have not shown any hazard.
As with all drugs during pregnancy care should be taken in assessing the risk to benefit ratio. Administration during labor may cause respiratory depression in the new-born infant.
Pethidine crosses the placental barrier and is excreted in breast milk. Patients should be advised to discontinue breastfeeding during treatment with pethidine
4.7 Effects on ability to drive and use machines
Patients should not drive or use machines while taking pethidine as it may cause drowsiness and reduce alertness.
The ability to drive or use machines may be severely affected during and for some time after administration of pethidine. This medicine can impair cognitive function and can affect a patient’s ability to drive safely. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act 1988. When prescribing this medicine, patients should be told:
• The medicine is likely to affect your ability to drive
• Do not drive until you know how the medicine affects you
• It is an offense to drive while under the influence of this medicine
• However, you would not be committing an offense (called ‘statutory defense’)
o The medicine has been prescribed to treat a medical or dental problem and
o You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and
o It was not affecting your ability to drive safely
4.8 Undesirable effects
There are no modern clinical studies available that can be used to determine the frequency of undesirable effects. Therefore, all the undesirable effects listed are classified as “frequency unknown” (cannot be estimated from the available data).
The undesirable effects listed below include class effects for opioid analgesics and effects related to the pharmacologically active metabolite, norpethidine.
System Organ Class
Immune system disorders
General hypersensitivity reactions
Dependence, confusion, mood altered, mild euphoria, hallucinations, dysphoria
Nervous system disorders
Drowsiness, dizziness, tremor, convulsions, headache, fainting, CNS excitation
Dry eye, miosis, corneal reflex decreased
Ear and labyrinth disorders
Tachycardia, bradycardia, palpitations
Orthostatic hypotension, flushing, hypotension, hypertension, vasodilation
Respiratory, thoracic and mediastinal disorders
Nausea, vomiting, dry mouth, constipation
Biliary or Ureteric spasm
Skin & subcutaneous tissue disorders
Sweating, rash, urticaria, pruritus
Musculoskeletal and connective tissue disorders
Respiratory depression, CNS depression with extreme somnolence progressing to incoordination, stupor or coma, convulsions, CNS stimulation, cyanosis, miosis, skeletal muscle flaccidity or tremors, cold, clammy skin, hypothermia, bradycardia, and hypotension.
In severe overdosage, apnoea, circulatory collapse, pulmonary edema, mydriasis, cardiac arrest, and death may occur.
Treatment is supportive. A patent airway must be established with assisted or controlled ventilation. If signs of CNS toxicity are exhibited the use of pethidine should be discontinued. Narcotic antagonists may be required if there is evidence of significant respiratory or cardiovascular depression.
Naloxone should be given intravenously as soon as possible and repeated every 2-3 minutes if necessary (refer to naloxone product literature for details).
Anti-convulsive therapy, oxygen, intravenous fluids, vasopressors, and other supportive measures should be employed as indicated.
5. Pharmacological properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Analgesics – Phenylpiperidine derivatives.
ATC code: NO2A B.
Pethidine is a synthetic opioid analgesic similar to morphine although less potent and shorter acting. Its analgesic effect usually lasts for 2 to 4 hours. The analgesic effect occurs after about 10 minutes following parenteral administration. It acts on the CNS system and smooth muscles via the peripheral nervous system. However, it has a weaker action on smooth muscle than morphine and therefore has less effect on cough, bowel motility, biliary tone and secretion of pituitary hormones. Pethidine also causes the release of histamine from mast cells resulting in a number of allergic-type reactions.
Pethidine is a narcotic analgesic with similar actions to morphine.
5.2 Pharmacokinetic properties
Pethidine is rapidly absorbed following intramuscular or subcutaneous injection, however, there are wide inter-individual variations. It is widely distributed in the tissues with a volume of distribution of 200-300 liters and is extensively protein bound (60-80%).
Pethidine is metabolized in the liver and excreted via the urine (70% in 24 hours). One of the metabolites, norpethidine, is pharmacologically active and its accumulation can result in toxicity. Urinary excretion is pH-dependent, the lower the pH the greater the clearance. At normal urinary pH, only a small amount of pethidine is excreted unchanged.
Pethidine has a plasma elimination half-life of about 3 to 6 hours. The metabolite norpethidine is eliminated more slowly with a half-life of up to 20 hours and may accumulate with chronic use, especially in the presence of renal impairment.
Pethidine crosses the placenta and is excreted in breast milk.
Both pethidine and norpethidine cross the blood/brain barrier and are found in the cerebrospinal fluid.
5.3 Preclinical safety data
No additional pre-clinical data of relevance to the prescriber.
6. Pharmaceutical particulars
6.1 List of excipients
Sodium Hydroxide may be added to adjust the pH.
Water for Injection
In the absence of incompatibility studies, Pethidine must not be mixed with other medicinal products.
Pethidine is incompatible with barbiturate salts and with other drugs including aminophylline, heparin sodium, methicillin sodium, morphine sulfate, nitrofurantoin sodium, phenytoin sodium, sulphadiazine sodium, sodium iodide, sulphafurazole diethanolamine. Incompatibility has also been observed between pethidine hydrochloride and acyclovir sodium, imipenem, frusemide, and idarubicin.
Color changes or precipitation have been observed on mixing pethidine with the following drugs, minocycline hydrochloride, tetracycline hydrochloride, cefoperazone sodium, mezlocillin sodium, nafcillin sodium, and liposomal doxorubicin hydrochloride.
6.3 Shelf life
6.4 Special precautions for storage
Store below 25°C.
Keep the ampoules in the outer carton.
Protect from light.
6.5 Nature and contents of the container
1ml and 2ml in colorless Type 1 neutral glass ampoules. Fusion sealed. Packed in cartons of 10 ampoules.
6.6 Special precautions for disposal and another handling
Pethidine is controlled under the Misuse of Drugs Act 1971 (Schedule 2).
1000 Amps, 120 Amps, 2000 Amps, 250 Amps, 500 Amps, 5000 Amps