Indication
Prevention
of atherosclerotic events in patients with history of symptomatic
atherosclerotic diseases (ischemic stroke, myocardial infarction or acute
coronary syndrome).
Dosage
and Administration
Once
daily.
Contraindication
and Precaution
Hypersensitivity
to any of the components or NSAIDs. Active pathological bleeding such as peptic
ulcer or intracranial hemorrhage or bleeding disorders T7-T10 spinal segments.
With the patient receiving the injection in the horizontal position and then
turned supine, the blockade spreads to T4-T7 spinal segments. It should be
understood that the level of spinal anesthesia achieved with any local
anesthetic can be unpredictable in
a
given patient. The Effects of Anespine exceeding 4 ml have not yet been studied
and such volumes can therefore not be recommended.
Contraindication & Precaution
Spinal anesthesia should only be undertaken by clinicians with
the necessary knowledge and experience. Patients with hypovolemia due to any
cause can develop sudden and severe hypotension during spinal
anesthesia.
It is contraindicated in patients with a known hypersensitivity to it or to any
local anesthetic agent of the amide type. The following conditions preclude the
use of spinal anesthesia: severe haemorrhage,
severe
hypotension or shock and arrhythmias, such as complete heart block, which
severely restrict cardiac output.
Side Effect
The safety of Bupivacaine is comparable to that of other local anesthetics
used for spinal anesthesia. In rare cases Bupivacaine has been associated
with
allergic reactions and anaphylactic shock. Spinal anesthesia itself can cause hypotension
and bradycardia due to sympathetic blockade and/or vasovagal fainting. Systemic
adverse reactions are characterized by numbness
of thetongue, Lightheadedness, dizziness and
tremors,
followed by convulsions and cardiovascular disorders.
Use in Pregnancy & Lactation
Bupivacaine
enters the mother’s milk but in such small quantities that there is generally
no risk of affecting the child at therapeutic dose levels. There is no may be
encountered during Losartan potassium treatment.
Use in Pregnancy & Lactation
Losartan potassium should not be used in pregnancy and if
pregnancy is detected Losartan potassium should be discontinued as soon as
possible. Losartan potassium should not be used in lactating mother.
Drug Interaction
No drug interaction of clinical significance has been identified.
Preparation: 25 mg,
50 mg & 100 mg Tablet.
0 comments:
Post a Comment