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Maximum Flu Strength Caplets

Document: spc-doc_PL 29831-0436 change

SUMMARY OF PRODUCT CHARACTERISTICS

1 NAME OF THE MEDICINAL PRODUCT

Maximum Flu Strength Caplets

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Paracetamol    500mg

Caffeine    25mg

Phenylephrine hydrochloride 6mg

3 PHARMACEUTICAL FORM

Tablets

White, coated, capsule-shaped tablets.

4 CLINICAL PARTICULARS

4.1    Therapeutic indications

Adults: For the relief of nasal congestion and congestion of mucous membranes of the upper respiratory tract associated with the common cold, and relief of cold and influenza, including relief of aches and pains, sore throat, headache, fatigue and drowsiness, and lowering of temperature.

Children of 6-12 years of age: Indicated as above.

4.2    Posology and method of administration

For oral administration. Swallow whole with water. Do not chew.

Adults and children over 12 years: 1 to 2 tablets every 4-6 hours. Maximum of 8 tablets in any 24 hour period. The dose should not be repeated more frequently than every 4 hours. Do not take for more than 3 days without consulting a doctor.

Children between 6-12 years: 1 tablet every 4-6 hours. Maximum of 4 tablets in any 24 hour period. Not to be used for more than 3 days without the advice of a doctor. Parents or carers should seek medical attention if the child’s condition deteriorates during treatment.

Maximum Flu Strength Caplets are contraindicated in children under the age of 6 years (see section 4.3)

4.3 Contraindications

Hypersensitivity to paracetamol, caffeine, phenylephrine or to any of the excipients. Not to be used in children under the age of 6 years.

Caffeine:

Do not give to patients with a history of peptic ulceration.

Phenylephrine hydrochloride

•    Hyper susceptible patients

•    Hyperthyroidism

•    Aneurysm

•    Arteriosclerosis

•    Phaeochromocytoma

•    Cardiovascular disease including hypertension

•    Prostatic enlargement

•    Diabetes mellitus

•    Closed angle glaucoma

•    Concomitant use of other sympathomimetic decongestants

•    Beta-blockers - (see section 4.5)

•    Monoamine oxidase inhibitors (MAOIs), including moclobemide (or within 14 days of stopping treatment, see section 4.5)

4.4 Special warnings and precautions for use Paracetamol

Care is advised in the administration of paracetamol to patients with renal or hepatic impairment. The hazards of overdose are greater in those with alcoholic liver disease. Paracetamol should be given with care to patients with alcoholic dependence. Paracetamol is well tolerated by the majority of people with asthma. However, a small percentage of aspirin sensitive asthmatics are also sensitive to paracetamol. The likelihood of a reaction to paracetamol increases with a patient’s level of sensitivity to aspirin (see also 4.8 Undesirable Effects).

Caffeine

Care is advised in the administration of caffeine to patients with cardiac disease. Phenylephrine

• Care is advised in the administration of phenylephrine in patients with

cardiovascular conditions such as occlusive vascular disease, Prinzmetal’s angina,

thromboembolic disorders, following myocardial infarction or a history of ischaemic heart disease.

• If any of the following occur, Maximum Flu Strength Caplets should be stopped

•    Hallucinations

•    Restlessness

•    Sleep disturbances

The following warnings appear in the leaflet and on the label:

Label-

Do not take with any other paracetamol-containing products.

Immediate medical advice should be sought in the event of an overdose, even if you feel well.


Leaflet-

Immediate medical advice should be sought in the event of an overdose even if you feel well, because of the risk of delayed, serious liver damage.

General points:

Do not exceed the recommended dose If symptoms persist consult a doctor.

Do not give to children under 6 years of age.

Keep out of the reach and sight of children.

Do not take for more than three days unless your doctor agrees.

Patients should be advised not to take other paracetamol-containing products concurrently.

4.5 Interaction with other medicinal products and other forms of interaction Paracetamol

Alcohol: Paracetamol should be given with care to patients with alcohol dependence (see Section 4.4).

Analgesics: Diflunisal increases blood concentrations of paracetamol.

Anion-exchange resins: Absorption reduced by colestyramine; administration should be separated by at least one hour.

Antibacterials: Isoniazid may increase the risk of hepatotoxicity with therapeutic doses of paracetamol.

Anticoagulants: The anticoagulant effect of warfarin and other coumarins may be enhanced by prolonged regular use of paracetamol, with increased risk of bleeding; occasional doses have no significant effect.

Antiepileptics: Carbamazepine, phenobarbital, phenytoin and primidone can reduce the effects of paracetamol and increase the risk of hepatotoxicity. Paracetamol may increase lamotrigine metabolism.

Motility stimulants: The speed of absorption of paracetamol may be increased by metoclopramide or domperidone

Oral Contraceptives: Paracetamol is cleared from the body more quickly in women taking oral contraceptives and the analgesic effects may be reduced.

Uricosurics: Probenecid can reduce the loss of paracetamol from the body.

Caffeine

Antibacterials: Some quinolone antibiotics can reduce the clearance of caffeine and prolong its plasma half-life.

Antidepressants: Fluvoxamine can reduce the clearance of caffeine and increase its stimulant and side effects.

Antiepileptics: Phenytoin may increase the clearance of caffeine.

Benzodiazepines: Caffeine can reduce the sedative effects of diazepam.

Disulfiram: may reduce the clearance of caffeine.

Lithium: Caffeine may increase the clearance of lithium.

Mexiletine: may reduce the clearance of caffeine.

Oestrogens and progestogens: Oral contraceptives or oestrogen replacement therapy may reduce the clearance of caffeine.

Phenylpropanolamine: Concomitant administration may increase blood pressure, resulting in hypertensive crises in a few susceptible individuals. Manic psychosis has occurred. Phenylpropanolamine can increase serum caffeine levels.

Theophylline: concomitant administration can increase plasma theophylline and plasma caffeine levels.

Phenylephrine Hydrochloride

Anticholinergic drugs: Maximum Flu Strength Caplets enhance the effects of anticholinergic drugs (such as TCAs).

There is an increased risk of hypertension when used with atropine.

Antidepressants: Maximum Flu Strength Caplets should not be given to patients treated with monoamine oxidase inhibitors (MAOIs) and/or RIMAs (such as moclobemide), or within 14 days of stopping treatment with MAOIs: increased risk of hypertensive crisis (see Section 4.3 Contraindications).

There is an increased risk of hypertension when used with tricyclic antidepressants e.g. imipramine.

Antihypertensives (including adrenergic neurone blockers and beta-blockers): Maximum Flu Strength Caplets may block the hypotensive effect. Adrenergic neurone blockers may enhance the hypertensive effect of phenylephrine.

Cardiac glycosides: increased risk of dysrhythmias.

Appetite suppressants and amphetamine-like psychostimulants: risk of hypertension.

Antimigraine drugs: Ergot alkaloids (ergotamine and methysergide):-increased the risk of ergotism, including vasoconstriction and hypertension.

Oxytocics: there is a potential increased risk of hypertension with oxytocin.

Sympathomimetics: concomitant use with other sympathomimetics can increase the hypertensive effect.

4.6 Pregnancy and lactation Paracetamol:

Epidemiological studies in human pregnancy have shown no ill effects due to paracetamol use in the recommended dosage, but patients should follow the advice of their doctor regarding its use.

Paracetamol is excreted in breast milk but not in a clinically significant amount. Available published data do not contraindicate breast-feeding.

Caffeine:

Taken during pregnancy, it appears that the half-life of caffeine is prolonged. This is a possible contributing factor in hypermesis gravidarum. Caffeine crosses the placenta, and foetal blood and tissue levels similar to maternal concentrations are achieved. Caffeine intake during pregnancy should be kept to a minimum.

Caffeine is excreted in breast milk, but with moderate intake amounts are probably too low to be clinically significant. Regular intake of large amounts of caffeine can affect the nursing infant.

Phenylephrine hydrochloride:

The safety of phenylephrine during pregnancy has not been established but there is some evidence suggesting a possible association of foetal abnormalities with first trimester exposure to phenylephrine. As an alpha-adrenoceptor stimulant, it might provoke uterine changes, which can result in foetal asphyxia. There is no information on the excretion of phenylephrine into breast milk; however no clinical problems have been documented.

In view of the above, Flu Strength Cold Relief Caplets should be avoided during pregnancy and lactation unless prescribed by a doctor.

4.7 Effects on ability to drive and use machines

Paracetamol:

None.

Caffeine:

None.

Phenylephrine Hydrochloride:

May cause dizziness, if affected, do not drive or operate machinery.

4.8 Undesirable effects Paracetamol:

Adverse effects of paracetamol are rare.

Haematological: There have been reports of blood dyscrasias including thrombocytopenia and agranulocytosis, but these were not necessarily causally related to paracetamol.

Immune system: Hypersensitivity including skin rash may occur. A small percentage of aspirin-sensitive asthmatics are also sensitive to paracetamol. In such cases, the deterioration in respiratory function induced by paracetamol is milder and shorter than with aspirin (see also 4.4 Special warnings and precautions for use).

Renal and urinary disorders: Nephropathy has been associated with chronic high dose use.

Caffeine:

Tremor, anxiety and insomnia may be experienced. Withdrawal may induce headache. Large doses may cause restlessness, excitement and extrasystoles.

Phenylephrine Hydrochloride:

Cardiovascular effects:

•    Tachycardia/palpitations

•    Other cardiac dysrhythmias

•    Hypertension with headache

•    Reflex bradycardia

CNS effects:

•    Irritability

•    Anxiety

•    Restlessness

•    Excitability

•    Insomnia

•    Hallucinations and paranoid delusions

Skin reactions including rash:

Hypersensitivity reactions - including that cross-sensitivity may occur with other sympathomimetics.

Other reactions:

•    Nausea and /or vomiting

•    Headache

•    Dizziness

•    Difficulty in micturition and urinary retention

4.9 Overdose

Paracetamol

Liver damage is possible in adults who have taken 10g or more of paracetamol. Ingestion of 5g or more of paracetamol may lead to liver damage if the patient has risk factors (see below).

Risk Factors If the patient

a.    Is on long term treatment with carbamazepine, phenobarbital, phenytoin, primidone, rifampicin, St John’s Wort or other drugs that induce liver enzymes.

Or

b.    Regularly consumes ethanol in excess of recommended amounts.

Or

c.    Is likely to be glutathione deplete e.g. eating disorders, cystic fibrosis, HIV infection, starvation, cachexia.

Symptoms

Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur. In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema and death. Acute renal failure with acute tubular necrosis, strongly suggested by loin pain, haematuria and proteinuria, may develop even in the absence of severe liver damage. Cardiac arrhythmias and pancreatitis have been reported.

Treatment

Immediate treatment is essential in the management of paracetamol overdose. Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention. Symptoms may be limited to nausea or vomiting and may not reflect the severity of overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines, see BNF overdose section.

Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour. Plasma paracetamol concentration should be measured at 4 hours or later after ingestion (earlier concentrations are unreliable). Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however, the maximum protective effect is obtained up to eight hours post ingestion. The effectiveness of the antidote declines sharply after this time. If required the patient should be given intravenous N-acetylcysteine in line with the established dosage schedule. If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas, outside hospital. Management of patients who present with serious hepatic dysfunction beyond 24 hours from ingestion should be discussed with the NPIS or a liver unit.

Caffeine

Symptoms: Large doses may cause restlessness, excitement, muscle tremor, tinnitus, scintillating scotoma, tachycardia and extrasystoles. Emesis and convulsions may occur. No specific antidote. However, treatment is usually fluid therapy. Fatal poisoning is rare. If symptoms become apparent or overdose is suspected, consult a doctor immediately.

Phenylephrine Hydrochloride

Severe hypertension is possible. If overdose is suspected, consult your doctor immediately.

5    PHARMACOLOGICAL PROPERTIES

5.1    Pharmacodynamic properties

Paracetamol:

Paracetamol has analgesic and antipyretic properties. Analgesic effects are thought to be related to inhibition of prostaglandin synthesis. An antipyretic effect has been demonstrated where fever exists but normal body temperature is not lowered. The drug acts on the hypothalamus to produce antipyresis; heat dissipation is increased as a result of vasodilation and increased peripheral blood flow.

The failure of paracetamol to exert anti-inflammatory activity may be attributed to the fact that it is only a weak inhibitor of cyclo-oxygenase in the presence of the high concentrations of peroxides that are found in inflammatory lesions. Further, paracetamol does not inhibit neutrophil activation as do other NSAIDs.

Single or repeated therapeutic doses of paracetamol have no effect on the cardiovascular and respiratory systems, nor does the drug produce gastric irritation, erosion, or bleeding.

Phenylephrine:

Phenylephrine is a relatively selective *1-adrenoceptor agonist. It has weak *2-adrenoceptor agonist activity, some activity as a low cardioselective B-adrenoceptor agonist and minimal central stimulant activity. It is also termed a sympathomimetic vasoconstrictor. Most of the *1-stimulant activity is due to an indirect effect via release of noradrenaline. Sympathomimetic vasoconstriction forms the basis of its decongestant actions, for which it is most widely used.

Caffeine:

The primary effect of caffeine is central nervous system stimulation, mainly on the higher centres. This expressed in terms of increased vigilance, wakefulness, relief from fatigue, increased mental activity, improved performance and improved mood. Other effects include diuresis and increased cardiac output with peripheral vasodilation. Caffeine, a methylxanthine, exerts its pharmacological effects by increasing calcium permeability in the sarcoplasmic reticulum, inhibiting phosphodiesterase and promoting accumulation of cyclic AMP. Caffeine is also a competitive, non-selective antagonist at adenosine A1 and A2A receptors. Evidence suggests that adenosine receptor antagonism is the most important factor responsible for most pharmacological effects of methylxanthines in doses that are administered therapeutically.

5.2 Pharmacokinetic properties

Paracetamol:

Paracetamol is rapidly and almost completely absorbed from the gastrointestinal tract, with peak plasma concentrations reached in 10-15 minutes after oral dosing. Dissolution and gastric emptying are rate-limiting steps; the mean half-time of absorption from upper small intestine is within minutes. The absolute oral bioavailability is about 80% and is independent of dose in the range 5 to 20 mg/kg. Oral bioavailability of paracetamol is subject to first pass metabolism. Paracetamol is rapidly and uniformly distributed into most body tissues. About 25% of paracetamol in blood is bound to plasma proteins. The mean plasma paracetamol half-life following a therapeutic dose is about 2.3 hours in healthy adults, with a range of 1.5 - 3 hours. Paracetamol crosses the placenta and is present in breast milk.

After therapeutic doses, 90 - 100% of the drug may be recovered in the urine within the first day, primarily after hepatic conjugation with glucuronic acid (about 60%), sulphuric acid (about 35%) or cysteine (about 3%); small amounts of hydroxylated and deacetylated metabolites have also been detected. A small proportion of paracetamol undergoes P450-mediated N-hydroxylation to form N-acetyl-benzoquinoneimine, a highly reactive intermediate. After large doses of paracetamol, this metabolite is formed in amounts sufficient to deplete hepatic glutathione. Under these circumstances, reaction with sulphydryl groups in hepatic proteins is increased and hepatic necrosis can result. Renal clearance is about 10 ml/min.

Phenylephrine:

Phenylephrine is readily absorbed after oral administration but is subject to extensive presystemic metabolism, much of which occurs in the enterocytes. As a consequence, systemic bioavailability is only about 40%. Following administration, peak plasma concentrations are achieved in 1-2 h. The mean plasma half-life is in the range 2-3 h. Penetration into the brain appears to be minimal.

Phenylephrine undergoes extensive biotransformation in the liver. Both phenylephrine and its metabolites are excreted in urine, with less than 20% as unchanged drug. The principal routes of metabolism are to sulphate conjugates, formed largely in the gut wall, and deamination by monoamine oxidase. There are no data on the extent of protein binding. Excretion in breast milk appears to be minimal.

Caffeine:

Caffeine is absorbed readily after oral administration to the extent of 99%, peak plasma levels occur in 15-45 min. The half-life of caffeine in plasma shows considerable variation with the reported values ranging from 3.0-7.5 hours. It is widely and rapidly distributed throughout the body, and passes readily into the central nervous system and saliva. Approximately 17% of the drug is bound to plasma proteins. Caffeine crosses the placenta and has been shown to distribute into milk in a milk-to-serum concentration of 0.52.

In adults, caffeine is metabolised almost completely in the liver via oxidation, demethylation, and acetylation, and is excreted in the urine as 1-methyluric acid, 1-methylxanthine and other metabolites with only about 1% unchanged. Neonates have a greatly reduced capacity to metabolise caffeine and it is largely excreted unchanged in the urine until hepatic metabolism becomes significantly developed.

5.3 Preclinical safety data

The active ingredients have been in widespread use for many years and have a well established therapeutic profile. There is no further data of relevance to the prescriber in addition to than that presented in the other sections of the SmPC.

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Povidone

Nipasept (contains E214, E216, E218)

Crospovidone

Magnesium stearate

Stearic acid

Talc

Colloidal silicon dioxide

Coating contains:

Hydroxypropyl methylcellulose Polyethylene glycol

6.2 Incompatibilities

None

6.3 Shelf life

2 years from the date of manufacture.

6.4    Special precautions for storage

Do not store above 25°C.

6.5    Nature and contents of container Polypropylene/polyethylene containers:

Pack sizes:    28, 32 (Pharmacy)

Blister Packs:

Pack sizes:    24, 28, 32 (Pharmacy)

Blister strips consist of a 35gsm paper/9p soft tempered aluminium foil lid and 250p PVC film base in cartons.

6.6 Special precautions for disposal

No special instructions.

7    MARKETING AUTHORISATION HOLDER

Wockhardt UK Ltd Ash Road North Wrexham LL13 9UF UK.

8    MARKETING AUTHORISATION NUMBER(S)

PL 29831/0436

9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

19 September 2001

10 DATE OF REVISION OF THE TEXT

17/08/2009