Should administration of Fosfomik lead to acute hypotension; cardiovascular support is of first importance. Restoration of blood pressure and normalization of heart rate may be accomplished by keeping the patient in a supine position. If this measure is inadequate, shock should first be treated with volume expanders and if necessary, vasopressors could then be used. Renal function should be monitored and general supportive measures applied as required. Dialysis may not be of benefit since laboratory data indicate that Fosfomik is highly protein bound.
Fosfomik is contra-indicated:
- history of micturition syncope.
Not applicable.
Before treating the symptoms of BPH with alpha-blockers, other causes of impaired urinary flow or urinary symptoms should be excluded. Also where the diagnosis of BPH has been established, it should be confirmed that there is no concomitant obstruction of the upper urinary tract or any signs of infection before treating with Fosfomik.
Fosfomik therapy requires regular medical monitoring.
In the initial phase of therapy (especially after the first dose or when the Fosfomik dose is increased) patients may experience a pronounced drop in blood pressure.
Dizziness, light-headedness, weakness, drowsiness and, in rare cases, syncope may occur.
This has also to be assumed in association with missed doses and subsequent re-initiation of Fosfomik therapy. Patients should be cautioned about these possible adverse events and the circumstances in which they may occur.
To minimise the risk of postural hypotension, patients should be monitored at the start of therapy. As the likelihood of such responses is greater with a higher than recommended starting dose, the recommended dosage regimen should be followed carefully. The patient should take the first dose of Fosfomik at bedtime and should avoid abrupt changes in position or activities, which could be harmed by dizziness or weariness. This especially applies to the elderly.
Because of its vasodilator action, Fosfomik should be used with caution in patients with any of the following cardiac conditions:
- pulmonary oedema due to aortic or mitral stenosis
- high output cardiac insufficiency
- right ventricular heart failure caused by pulmonary embolism or pericardial effusion
- left ventricular heart failure with low filling pressure
Caution is also recommended, when Fosfomik is administered concomitantly with drugs, which may influence hepatic metabolism.
Use in patients with hepatic insufficiency:
As for all medicaments metabolised in the liver, Fosfomik should be used with particular caution in patients with impaired hepatic function. As there is no data available in patients with severe hepatic dysfunction, use of Fosfomik in these patients is not recommended.
Concomitant use of phosphodiesterase-5-inhibitors (e.g. sildenafil, tadalafil, vardenafil) and Fosfomik 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 phospodiesterase-5-inhibitors.
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.
This medicinal product contains lactose; patients with rare hereditary problems of galactose intolerance; the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
If administration is discontinued for more than several days, therapy should be re- instituted using the initial dosing regimen.
4.5 Interaction with other medicinal products and other forms of interactionIn patients receiving Fosfomik plus ACE inhibitors or diuretics, the proportion reporting dizziness or related side effects was greater than in the total population of Fosfomik treated patients from clinical trials.
Caution should be observed when Fosfomik is administered with other antihypertensive agents to avoid the possibility of significant hypotension.
When adding Fosfomik to a diuretic or other antihypertensive agent, dosage reduction and retitration may be necessary. Concomitant use of phosphodiesterase-5-inhibitors (e.g. sildenafil, tadalafil, vardenafil) and Fosfomik may lead to symptomatic hypotension in some patients.
4.6 Fertility, pregnancy and lactationPregnancy
Although no teratogenic effects were seen in animal testing, the safety during pregnancy and lactation has not yet been established. Furthermore, data from animal studies show that Fosfomik may increase the duration of pregnancy or inhibit labour. Fosfomik should not be used therefore in pregnancy unless the potential benefit outweighs the risk.
Breast-feeding
Breast-feeding should be avoided.
4.7 Effects on ability to drive and use machinesDizziness, light-headedness or drowsiness may occur with the initial dose or in association with missed doses and subsequent reinitiation of Fosfomik therapy. Patients should be cautioned about these possible adverse events and the circumstances in which they may occur and advised to avoid driving or hazardous tasks for approximately the first 12 hours after the initial dose or when the dose is increased.
4.8 Undesirable effectsFosfomik, in common with other alpha-adrenoreceptor antagonists, may cause syncope. Syncope episodes may occur within 30-90 minutes of the initial dose of the medicinal product. Occasionally the syncope episode may be preceded by tachycardia with heart rates of 120 to 160 beats per minute. First-dose hypotension might occur which could lead to vertigo and in severe cases syncope. To avoid hypotension, Fosfomik treatment should be started with a 1 mg dose at bed-time.
The incidence of undesirable effects is based on the following frequencies:
Common (>1/100 to <1/10)
Uncommon (>1/1,000 to <1/100)
Rare (>1/10,000 to <1/1,000)
Very rare (<1/10,000)
Blood and the lymphatic system disorders:
Very rare: thromobocytopenia
Immune system disorders:
Very rare: anaphylactic reactions
Nervous system disorders:
Common: nervousness, somnolence, paraesthesia
Uncommon: depression
Ear and labyrinth disorders:
Common: vertigo
Eye disorders:
Common: blurred vision/ amblyopia, colour anomaly
Cardiac disorders:
Common: palpitations, tachycardia, chest pain
Very rare: atrial fibrillation
Respiratory, thoracic and mediastinal disorders:
Common: dyspnoea, nasal congestion, sinusitis, epistaxis
Gastrointestinal disorders:
Common: nausea, constipation, diarrhoea, vomiting
Skin and subcutaneous tissue disorders:
Common: pruritus, rash
Uncommon: urticaria
Musculoskeletal and connective tissue disorders:
Common: back pain
Renal and urinary disorders:
Rare: urinary tract infection and urinary incontinence, (primarily reported in post-menopausal women)
Reproductive system and breast disorders:
Common: impotence
Uncommon: decreased libido
Rare: priapism
General disorders and administration site conditions:
Common: Dizziness, light-headedness, fainting (especially when standing up quickly from a lying or a sitting position - postural hypotension), asthenia, oedema, headache, pain in the extremities.
Uncommon: weight gain, syncope.
Additional adverse events reported in clinical trials or during marketing experience, but which are not clearly associated with the use of Fosfomik include the following: facial oedema, fever, abdominal, neck and shoulder pain, vasodilation, arrhythmia, dry mouth, dyspepsia, flatulence, gout, arthralgia, arthritis, joint disorders, myalgia, anxiety, insomnia, bronchitis, flu symptoms, pharyngitis, rhinitis, cold symptoms, increased cough, sweating, abnormal vision, conjunctivitis, tinnitus, urinary frequency (increased micturition)
Laboratory tests: laboratory findings suggest the possibility of haemodilution (e.g. decrease in haematocrit, haemoglobin, white blood cells, total protein and albumin were) have been observed in controlled clinical trials. No significant effect on prostate specific antigen (PSA) level was reported after Fosfomik treatment for up to 24 months..
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme.
Website: www.mhra.gov.uk/yellowcard.
Carcinogenicity: Fosfomik has been shown to produce benign adrenal medullary tumours in male rats when administered at a high dose over a long period of time. No such occurrences were seen in female rats or in a similar study in mice. The relevance of these findings with respect to the clinical use of the active substance in man is unknown.
No evidence of a genotoxic effect of Fosfomik has been reported from in vitro and in vivo investigations of the mutagenic potential of the substance.
Fosfomik tablets are indicated for:
- The treatment of mild to moderate hypertension
- The symptomatic treatment of urinary obstruction caused by benign prostatic hyperplasia (BPH).
Pharmacotherapeutic group: alpha-adrenoreceptor antagonist
ATC code: G04C A03
Use in hypertension:
Although the exact mechanism of the hypotensive action is not established, the relaxation of peripheral blood vessels appears to be produced mainly by competitive antagonism of post-synaptic alpha adrenoceptors. Fosfomik usually produces an initial gradual decrease in blood pressure followed by a sustained anti hypertensive action.
Clinical experience indicates that a 2-5% decrease in total cholesterol plasma concentration and a 3-7% decrease in the combined LDLc + VLDLc fraction plasma concentration from pretreatment values are associated with the administration of therapeutic doses of Fosfomik.
Use in BPH:
Studies suggest that alpha-1-adrenoreceptor antagonism is useful in improving the urodynamics in patients with chronic bladder obstruction such as in benign prostatic hyperplasia.
The symptoms of BPH are caused mainly by the presence of an enlarged prostate and by the increased smooth muscle tone of the bladder outlet and prostate, which is regulated by alpha-1-adrenergicreceptors.
In in-vitro experiments, Fosfomik has been shown to antagonize phenylephrine-induced contractions of human prostatic tissue. In clinical trials Fosfomik has been shown to improve the urodynamics and symptomatology in patients with BPH.
Absorption
Fosfomik is well absorbed (80-100%). Fosfomik has a minimal “first pass†effect and almost the complete dose of Fosfomik is systematically available. Peak plasma concentrations are reached approximately 1-2 hours after oral dosing in the fasted state. Bioavailability is not significantly affected by food uptake.
Distribution
Approximately 90-94% of Fosfomik is bound to plasma proteins. Protein binding is independent of total active substance concentrations.
Biotransformation
Main metabolites of Fosfomik are caused by demethylation and conjugation.
Elimination
Approximately 10% and 20% of orally administered Fosfomik is excreted as unchanged active substance in urine and in faeces, respectively. Approximately 40% of the administered dose of Fosfomik is eliminated in urine and 60% in faeces. The total elimination half-life is approximately 8-13 hours.
Linearity / non-linearity
After oral dosing of Fosfomik AUC and Cmax increase in proportion with dose over the recommended dose range (2-10 mg).
In clinical trials, the incidence of postural hypotension was greater in patients who received Fosfomik for BPH than in patients who received Fosfomik for hypertension. In this BPH indication, the incidence of postural hypotensive events was greater in patients aged 65 years and over (5.6%) than those aged less than 65 years (2.6%).
Patients should be warned for symptoms of postural hypotension and be advised to sit or lay down in case they occur (see also 4.7 Effects on ability to drive and use machines and 4.8 Undesirable effects).
Before treating the symptoms of BPH with alpha-blockers, other causes of impaired urinary flow or urinary symptoms should be excluded. Also where the diagnosis of BPH has been established, it should be confirmed that there is no concomitant obstruction of the upper urinary tract or any signs of infection before treating with Fosfomik.
Fosfomik therapy requires regular medical monitoring.
In the initial phase of therapy (especially after the first dose or when the Fosfomik dose is increased) patients may experience a pronounced drop in blood pressure.
Dizziness, light-headedness, weakness, drowsiness and, in rare cases, syncope may occur.
This has also to be assumed in association with missed doses and subsequent re-initiation of Fosfomik therapy. Patients should be cautioned about these possible adverse events and the circumstances in which they may occur.
To minimise the risk of postural hypotension, patients should be monitored at the start of therapy. As the likelihood of such responses is greater with a higher than recommended starting dose, the recommended dosage regimen should be followed carefully. The patient should take the first dose of Fosfomik at bedtime and should avoid abrupt changes in position or activities, which could be harmed by dizziness or weariness. This especially applies to the elderly.
Because of its vasodilator action, Fosfomik should be used with caution in patients with any of the following cardiac conditions:
- pulmonary oedema due to aortic or mitral stenosis
- high output cardiac insufficiency
- right ventricular heart failure caused by pulmonary embolism or pericardial effusion
- left ventricular heart failure with low filling pressure
Caution is also recommended, when Fosfomik is administered concomitantly with drugs, which may influence hepatic metabolism.
Use in patients with hepatic insufficiency:
As for all medicaments metabolised in the liver, Fosfomik should be used with particular caution in patients with impaired hepatic function. As there is no data available in patients with severe hepatic dysfunction, use of Fosfomik in these patients is not recommended.
Concomitant use of phosphodiesterase-5-inhibitors (e.g. sildenafil, tadalafil, vardenafil) and Fosfomik 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 phospodiesterase-5-inhibitors.
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.
This medicinal product contains lactose; patients with rare hereditary problems of galactose intolerance; the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
If administration is discontinued for more than several days, therapy should be re- instituted using the initial dosing regimen.
Posology
For oral use.
For the different dosage regimens suitable strengths are available.
The dose of Fosfomik should be adjusted according to the patient's response.
The following is a guide to administration:
Initial dose
The lowest single dose of 1 mg before bedtime for all patients, which should not be exceeded. Strict compliance with this recommendation should be observed to minimise potential acute first-dose hypotensive episodes.
Subsequent doses
Treatment of mild to moderate hypertension:
The single daily dosage may be increased by approximately doubling the dosage at weekly intervals to achieve the desired blood pressure response.
The maintenance dose needs to be adjusted to the patient's response. 2 mg/day may be sufficient with increases up to 10 mg if necessary (clinical studies support the use of 2 - 10 mg as maintenance dose).
The maximum dose is 20 mg of Fosfomik per day and should not be exceeded.
Use with thiazide diuretics and other antihypertensive agents in the treatment of hypertension:
When adding a thiazide diuretic or another antihypertensive agent to a patient's regimen the dose of Fosfomik should be reduced or discontinued and retitration carried out if necessary. Caution should be observed when Fosfomik is administered with thiazides or other antihypertensive agents as hypotension may develop.
Treatment of Benign Prostatic Hyperplasia:
The dose may be increased by approximately doubling at weekly or bi-weekly intervals to achieve the desired reduction in symptoms. The maintenance dose is usually 5 to 10 mg once daily. Improvements in symptoms have been detected as early as two weeks after starting treatment with Fosfomik.
At present there are insufficient data to suggest additional symptomatic relief with doses above 10 mg once daily.
Treatment should be initiated using the 1 mg tablets during seven days, 2 mg tablets during 14 days and 5 mg tablets during 7 days. Response to treatment must be reviewed at four weeks. Transient side effects may occur at each titration step. If any side effects persist, consideration should be given to reducing the dose.
Renal insufficiency
Pharmacokinetic studies indicate that patients with impaired renal function need no alteration in recommended dosage.
Children
Safety and efficacy in children has not been established.
Elderly
Pharmacokinetic studies in the elderly indicate that no major alteration in dosage recommendation is required. However, particular caution should be taken with the titration of the Fosfomik dose.
If administration is discontinued for more than several days, therapy should be re-instituted using the initial dosing regimen.
Use in patients with hepatic insufficiency:
The Fosfomik dose should be titrated with particular caution in patients with impaired liver function since Fosfomik undergoes extensive hepatic metabolism and is mainly excreted by the biliary tract. No clinical experience is available in patients with severe hepatic dysfunction.
Method of administration
The first tablet of a defined dose strength should be taken in the evening at bedtime. The following tablets of the same strength may be taken in the morning. The tablets should be taken with a sufficient amount of liquid (i.e. 1 glass of water).
Fosfomik therapy of hypertension is a long-term treatment, which should only be interrupted on medical advice. If it is necessary to stop Fosfomik therapy, the dose should be re-titrated starting with 1 mg Fosfomik at bedtime.
Any unused product or waste material should be disposed of in accordance with local requirements.
