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CIMETIDINE INCREASES ITS PLASMA CONCENTRATION AND HENCE BIOAVAILABILITY
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METOCLOPRAMIDE EFFECTS ON G.I. MOTILITY ARE ANTAGONISED BY THE DRUG
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PANTAZOCINE MAY CAUSE INCREASED RISK OF RESPIRATORY DEPRESSION & HYPOTENSION
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CO-ADMINISTRATION MAY INCREASE CHANCES OF POSTOPERATIVE RESPIRATORY DEPRESSION OR ENHANCE IT
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CO-ADMINISTRATION CAN LEAD TO REDUCED EFFECTS OF PEGVISOMANT, SO HIGHER DOSES ARE NEEDED TO ACHIEVE RESULTS
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INCREASED HYPOTENSIVE EFFECT IS SEEN
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OPIOD ANALGESICS IN HIGH DOSE MAY RESULT IN DROP IN HEART RATE AND CARDIAC OUTPUT
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OPIATES DELAY ABSORPTION DUE TO SLOW GASTRIC EMPTYING
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MAOI INHIBIT THE METABOLISM OF SYMPATHOMIMETICS WHICH CAN LEAD TO DANGEROUS ENHANCEMENT OF THEIR PRESSOR EFFECTS CAUSING HEADACHE, HIGH BLOOD PRESSURE / HYPERTENSIVE CRISIS. A VARIETY OF NEUROLOGICAL TOXIC EFFECTS & MALIGNANT HYPERPYREXIA CAN OCCUR
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAOI ON CONCURRENT ADMINISTRATION MAY CAUSE MARKED HYPERPYREXIA, CONVULSION & COMA. HENCE SHOULD NOT BE USED WITHIN 2 WEEKS OF STOPPING MAOIS
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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MAY INCREASE DROWSINESS EFFECT
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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CONCURRENT ADMINISTRATION MAY CAUSE BRADYCARDIA, MYOCARDIAL DEPRESSION OR A.V. BLOCK
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KETAMINE EFFECT IS PROLONGED WITH SUBSEQUENT DELAY IN RECOVERY DUE TO CONCOMITANT USE
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CO-ADMINISTRATION WITH A PURE AGONIST OPIOID ANAGESIC LIKE LEVORPHANOL IS NOT RECOMMENDED
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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ANTICOAGULANT EFFECT IS INCREASED OF ORAL ANTICOAGULANTS
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RIFAMPICIN MAY ACCELERATES METABOLISM OF THE DRUG & MAY CAUSE DECREASED PLASMA CONCENTRATION
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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INCREASED SEDATIVE EFFECT
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