Ancor is not recommended for the emergency treatment of
hypertensive crises.
* রেজিস্টার্ডচিকিৎসকেরপরামর্শমোতাবেকঔষধসেবনকরুন'*
Interaction
Other β-blocking Agents: Ancor fumarate should not be
combined with other β-blocking agents.
Catecholamine-Depleting Drugs: Patients receiving
catecholamine-depleting drugs, such as reserpine or guanethidine, should be
monitored closely because the added β-adrenergic blocking action of bisoprolol
fumarate may produce excessive reduction of sympathetic activity.
Centrally Active Antihypertensive Agents: β-blockers may
exacerbate the rebound hypertension which can follow the withdrawal of
clonidine. If the two drugs are coadministered, the β-blocker should be
withdrawn several days before discontinuing clonidine. If replacing clonidine
by β-blocker therapy, the introduction of β-blockers should be delayed for
several days after clonidine administration has stopped (see also prescribing
information for clonidine).
Antiarrhythmic Agents: Ancor fumarate should be used with
care when myocardial depressants or inhibitors of A-V conduction, such as
certain calcium antagonists (particularly of the phenyl alkylamine (verapamil)
and benzothiazepine (diltiazem) classes), or antiarrhythmic agents, such as
disopyramide, are used concurrently.
Calcium Channel Blockers: Combined use of β-blockers and
calcium channel blockers with negative inotropic effects can lead to
prolongation of S-A and A-V conduction, particularly in patients with impaired
ventricular function or conduction abnormalities. This may result in severe
hypotension, bradycardia and cardiac failure.
Contraindications
In patients with cardiogenic shock, overt heart failure,
second or third degree A-V block, right ventricular failure secondary to
pulmonary hypertension and sinus bradycardia.
Side Effects
Medicines and their possible side effects can affect
individual people in different ways. The following are some of the side effects
that are known to be associated with this medicine. Just because a side effect
is stated here does not mean that all people using this medicine will
experience that or any side effect. Fatigue, dizziness, headache, disturbances
of the gut such as nausea, vomiting, diarrhea, constipation or abdominal pain.
Cold or numb extremities, e.g; hands and feet. Muscle weakness or cramps.
Slower than normal heart breathing difficulties due to a narrowing of the
airways (bronchospasm) in people with asthma or COPD.
Pregnancy & Lactation
Pregnancy: Bisoprolol fumarate was not teratogenic in rats
at doses up to 150 mg/kg/day, which is 375 times the maximum recommended human
daily dose. Bisoprolol fumarate was fetotoxic (increased late resorptions) at
50 mg/kg/day and maternotoxic (decreased food intake and body-weight gain) at
150 mg/kg/day. Bisoprolol fumarate was not teratogenic in rabbits at doses up
to 12.5 mg/kg/day, which is 31 times the maximum recommended human daily dose,
but was embryolethal (increased early resorptions) at 12.5 mg/kg/day. There are
no studies in pregnant women. Bisoprolol fumarate should be used during pregnancy
only if the potential benefit justifies the potential risk to the fetus.
Lactation: Small amounts of bisoprolol fumarate (<2% of
the dose) have been detected in the milk of lactating rats. It is not known
whether this drug is excreted in human milk. If use of bisoprolol fumarate is
considered essential, then mothers should stop nursing.
Precautions & Warnings
Impaired renal or hepatic function use caution in adjusting
the dose of Ancor in patients with renal or hepatic impairment. While taking
beta-blockers, patients with a history of severe anaphylactic reaction to a
variety of allergens may be more reactive to repeated challenge, accidental,
diagnostic, or therapeutic. Such patients may be unresponsive to the usual
doses of epinephrine used to treat allergic reactions.
Therapeutic Class
Anti adrenergic agent (Beta blockers), Beta-adrenoceptor
blocking drugs, Beta-blockers
Storage Conditions
Keep in a dry place away from light and heat. Keep out of
the reach of children.