1. Name Of The Medicinal Product
Doxadura 4 mg Tablets
Doxazosin 4 mg Tablets
2. Qualitative And Quantitative Composition
Doxazosin 4 mg contains 4.85 mg of doxazosin mesilate to the equivalent of 4 mg of the active constituent doxazosin.
For excipients, see section 6.1.
3. Pharmaceutical Form
Tablets.
Pink biconvex uncoated tablets, scored with a division mark on both sides and embossed with "DZS 4" on one side.
4. Clinical Particulars
4.1 Therapeutic Indications
Treatment of hypertension.
Doxazosin can be used as a mono-agent in the treatment of hypertension or in patients inadequately controlled on single antihypertensive therapy. Doxazosin tablets may be used in combination with thiazide diuretics, beta-adrenoceptor blocking agents, calcium antagonists or angiotensin
4.2 Posology And Method Of Administration
Doxazosin is used in a once daily regimen. The dose of Doxazosin should be adjusted according to the patient's response. The initial dose of Doxazosin should be 1 mg per day. Dosage may then be increased in intervals of 1 or 2 weeks to 2 mg and thereafter to 4 mg. If necessary, dosage can be further increased to 8 mg or the maximum recommended dose of 16 mg. Dosage may be increased until the desired blood pressure level is achieved, or until undesirable effects occur.
Children up to 16 years of age:
There is insufficient experience to recommend the use of Doxazosin tablets in children.
Elderly:
Normal adult dosage is recommended.
Renal insufficiency:
There is no change in pharmacokinetics of Doxazosin in patients with impaired renal function. Normal adult dosage is recommended. Doxazosin is not dialysable.
Hepatic insufficiency:
Up to now no studies have been performed with Doxazosin in patients with liver impairment. Since Doxazosin is extensively metabolised in the liver, it should be used with care in such patients.
4.3 Contraindications
Doxazosin is contraindicated in:
• patients with a known hypersensitivity to quinazolines (e.g. prazosin, terazosin, doxazosin), or any of the excipients
• patients with a history of orthostatic hypotension
• patients with benign prostatic hyperplasia and concomitant congestion of the upper urinary tract, chronic urinary tract infection or bladder stones
• during lactation (see section 4.6 Pregnancy and Lactation).
Doxazosin is contraindicated as monotherapy in patients with either overflow bladder or anuria with or without progressive renal insufficiency.
4.4 Special Warnings And Precautions For Use
Initiation of Therapy: in relation to the alpha-blocking properties of doxazosin, patients may experience postural hypotension evidenced by dizziness and weakness, or rarely loss of consciousness (syncope), particularly with the commencement of therapy. Therefore, it is prudent medical practice to monitor blood pressure on initiation of therapy to minimise the potential for postural effects. The patient should be cautioned to avoid situations where injury could result should dizziness or weakness occur during the initiation of doxazosin therapy.
Use in patients with Acute Cardiac Conditions: as with any other vasodilatory anti-hypertensive agent it is prudent medical practice to advise caution when administering doxazosin to patients with the following acute cardiac conditions:
• pulmonary oedema due to aortic or mitral stenosis
• heart failure at high output
• right-sided heart failure due to pulmonary embolism or pericardial effusion
• left ventricular heart failure with low filling pressure.
Use in Hepatically Impaired Patients: as with any drug wholly metabolised by the liver, doxazosin should be administered with particular caution to patients with evidence of impaired hepatic function. Since there is no clinical experiences in patients with severe hepatic impairment, use in these patients is not recommended.
Use with PDE-5 inhibitors: concomitant administration of phosphodiesterase-5-inhibitors (e.g. sildenafil, tadalafil and vardenafil) and doxazosin may lead to symptomatic hypotension in some patients. In order to minimise the risk for developing postural hypotension the patient should be stable on the alpha-blocker therapy before initiating use of phosphodiesterase-5-inhibitors.
Furthermore, it is recommended to initiate phosphodiesterase-5-inhibitor treatment with the lowest possible dose and to respect a 6-hour time interval from intake of doxazosin. No studies have been conducted with doxazosin prolonged release formulations.
Use in patients undergoing cataract surgery: the Intraoperative Floppy Iris Syndrome (IFIS, a variant of small pupil syndrome) has been observed during cataract surgery in some patients on or previously treated with tamsulosin. Isolated reports have also been received with other alpha-1 blockers and the possibility of a class effect cannot be excluded. As IFIS may lead to increased procedural complications during the cataract operation, current or past use of alpha-1 blockers should be made known to the ophthalmic surgeon in advance of surgery.
Excipients: Doxadura tablets contain lactose. Therefore, they should not be administered to persons with rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.
The excipient E110 is known to cause allergic reactions, including asthma. Allergy is more common in persons who are allergic to aspirin. This excipient is only used in the 2mg and 4mg tablets.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
Concomitant use of phosphodiesterase-5-inhibitors (e.g. sildenafil, tadalafil and vardenafil) and doxazosin may lead to symptomatic hypotension in some patients (see section 4.4).
Most (98%) of plasma doxazosin is protein bound. In vitro data in human plasma indicate that doxazosin has no effect on protein binding of digoxin, warfarin, phenytoin or indometacin. Conventional doxazosin has been administered without any adverse drug interaction in clinical experience with thiazide diuretics, furosemide, beta-blockers, non-steroidal anti-inflammatory drugs, antibiotics, oral hypoglycaemic drugs, uricosuric agents and anticoagulants. However data from formal drug/drug interactions studies are not present.
Doxazosin potentiates the blood pressure lowering activity of other alpha-blockers and other antihypertensives.
In an open-label, randomised, placebo-controlled trial in 22 healthy male volunteers, the administration of a single 1mg dose of doxazosin on day 1 of a four-day regiment of oral cimetidine (400mg twice daily) resulted in a 10% increase in mean AUC of doxazosin and no statistically significant changes in mean Cmax and mean half-life of doxazosin. The 10% increase in the mean AUC for doxazosin with cimetidine is within intersubject variation (27%) of the mean AUC of doxazosin with placebo.
4.6 Pregnancy And Lactation
As there are no adequate and well controlled studies in pregnant women, the safety of doxazosin during pregnancy has not been established. Accordingly, during pregnancy, doxazosin should be used only if the potential benefit outweighs the risk. Although no teratogenic effects were seen in animal testing, reduced foetal survival was observed in animals at high doses (see section 5.3 Preclinical Safety Data).
Doxazosin is contraindicated during lactation as the drug accumulates in milk of lactating rats and there is no information about the excretion of the drug into the milk of lactating women. Alternatively, mothers should stop breast-feeding when treatment with doxazosin is necessary (see section 5.3 Preclinical Safety Data).
4.7 Effects On Ability To Drive And Use Machines
The ability to engage in activities such as operating machinery or operating a motor vehicle may be impaired, especially when initiating therapy.
4.8 Undesirable Effects
Frequencies used are as follows: very common
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4.9 Overdose
Should overdose lead to hypotension, the patient should be immediately placed in a supine, head down position. Other supportive measures should be performed if thought appropriate in individual cases. Since doxazosin is highly protein bound, dialysis is not indicated.
If this measure is inadequate, shock should first be treated with volume expanders. If necessary, vasopressor should then be used. Renal function should be monitored and supported as needed.
5. Pharmacological Properties
5.1 Pharmacodynamic Properties
The ATC
Doxazosin is a selective postsynaptic α1
Maximal hypotensive effects occur after approximately 2 to 6 hours. With once daily dosing, clinically significant reductions in blood pressure are maintained throughout the day and at 24 hours post
After initiation of therapy increase in heart rate can occur, as well as changes in vasoactive hormones. After long
Doxazosin has a favourable effect on blood lipids: it decreases the LDL cholesterol, the total cholesterol and triglyceride levels. It increases the HDL/total cholesterol ratio.
Doxazosin has been shown to be free of adverse metabolic effects and is suitable for use in patients with obstructive airway disease, non
5.2 Pharmacokinetic Properties
Following oral administration of therapeutic doses of Doxazosin, peak plasma levels are reached after 2 to 4 hours. The bioavailability is approximately 63%. Doxazosin is 98% bound to plasma protein. Plasma elimination half
5.3 Preclinical Safety Data
There are no preclinical data of relevance to the prescriber other than those mentioned in previous sections.
6. Pharmaceutical Particulars
6.1 List Of Excipients
The following inactive ingredients are used in the tablets: microcrystalline cellulose, lactose monohydrate, sodium starch glycolate, magnesium stearate, sodium lauryl sulphate and colloidal silicon dioxide.
Sunset yellow FCF (E110) is an additional excipient present in the 2 and 4mg tablets.
6.2 Incompatibilities
Not applicable.
6.3 Shelf Life
The shelf life of the product is 3 years for all tablet strengths. The expiry date is printed on the package and on the blister ("EXP"). The first two digit numbers represent the month and the last four digit numbers represent the year. Do not use after this expiry date.
6.4 Special Precautions For Storage
Doxazosin tablets should be stored in the original package in a dry place. Do not store above 25ºC.
Keep all medicines out of the reach of children.
6.5 Nature And Contents Of Container
PVC/PVDC
Glass (type III) bottles or HDPE containers with child resistant closures (PP), with patient information leaflets attached.
6.6 Special Precautions For Disposal And Other Handling
Not applicable.
7. Marketing Authorisation Holder
Genus Pharmaceuticals Limited
T/A Genus Pharmaceuticals
Park View House
65 London Road
Newbury
Berkshire
RG14 1JN
United Kingdom
8. Marketing Authorisation Number(S)
PL 06831/0093
9. Date Of First Authorisation/Renewal Of The Authorisation
Date of first authorisation: 12 July 2002
Date of latest renewal: 25 March 2009
10. Date Of Revision Of The Text
13 May 2010
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