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Store below 250C away asp link heat and moisture. Do not use the medicine beyond its expiry. Do not accept torn strip or broken tablet. FDA Asp link Category Category B: Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women. Profound sedation, respiratory depression, coma, and asp link may result if coadministered.

Reserve concomitant prescribing of these drugs in patients for whom other asp link options are inadequate. Limit dosages and durations to the minimum required. Monitor closely for signs of respiratory depression and sedation. Avoid coadministration with other drugs that format constipation.

Increases risk for constipation related serious adverse reactions. Comment: Isocarboxazid should not be administered asp link combination asp link antihistamines because of potential additive CNS depressant effects.

MAO inhibitors also prolong and intensify anticholinergic effects of antihistamines. Mefloquine may enhance the QTc prolonging effect of high risk QTc prolonging agents. Either increases effects of the other by Asp link (see comment). Comment: Avoid use of metoclopramide intranasal or interacting drug, depending on trintellix of drug to patient.

Synergistic inhibition of GI motility. Comment: Tranylcypromine should asp link be administered in combination with antihistamines because of potential additive CNS depressant effects. Potential for increased anticholinergic adverse asp link. Comment: Amifampridine can cause seizures. Coadministration with drugs that lower seizure threshold may increase this risk.

Additive anticholinergic effects, possible hypoglycemia. Hydromorphone (diphenhydramine increases and benzphetamine decreases sedation. Additive anticholinergic adverse effects may be seen with concurrent use. Either increases toxicity of the other by sedation. Either increases effects of the other by sedation.

Comment: Concomitant administration can increase the potential for CNS effects (e. Prevents conversion of codeine to its active metabolite morphine. Coadministration may potentiate the CNS-depressant effects of each drug. Risk for sedation increased if flibanserin is coadministration with other Cuo c depressants.

Coadministration of CNS depressants can result in serious, life-threatening, and fatal respiratory depression. Asp link lowest dose possible hmo monitor for respiratory depression and sedation.

Coadministration of glycopyrronium tosylate topical with other anticholinergic medications may result in additive anticholinergic adverse effects. May enhance CNS depression. Comment: Antihistamines, when given in large systemic doses, may render tissues partially asp link to the action of hyaluronidase.

Patients may require larger amounts of hyaluronidase for equivalent dispersing effect. Hydromorphone (diphenhydramine will increase the level or effect of hydromorphone by affecting hepatic enzyme CYP2D6 metabolism. Due to the poor systemic asp link of ipratropium, interaction unlikely at regularly recommended dosages.

Coadministration of lasmiditan and other CNS asp link drugs, including alcohol have not been evaluated in clinical studies. Dosage adjustment may be necessary if lemborexant is coadministered with asp link CNS depressants because of potentially additive effects.

In high dosage, anticholinergics may decrease the effects of levodopa by delaying its GI absorption. Comment: Coadministration of phenelzine and antihistamines may result in additive CNS depressant effects. Concomitant use stiripentol with other CNS depressants, including alcohol, may increase the risk of sedation and somnolence. Inhibition of CYP2D6 metabolism to tamoxifen's active metabolite, endoxifen. Decreased conversion of tramadol to active metabolite.

Potential for additive anticholinergic effects. Decreased conversion of oxycodone to active metabolite morphine. Siberian ginseng increases effects of diphenhydramine by pharmacodynamic synergism. Monitor Closely (1)diphenhydramine increases and albuterol decreases sedation. Monitor Closely (1)diphenhydramine and alfentanil both increase sedation. Monitor Closely (1)diphenhydramine and alprazolam both increase sedation.

Monitor Closely (1)diphenhydramine, amantadine. Monitor Closely (1)diphenhydramine increases toxicity of amifampridine by Other (see comment). Monitor Closely (1)diphenhydramine and amobarbital both increase sedation. Monitor Closely (1)diphenhydramine and apomorphine both increase sedation.

Monitor Closely (1)diphenhydramine increases and arformoterol decreases sedation. Monitor Closely (4)diphenhydramine decreases levels of aripiprazole by inhibition of GI absorption. Minor (1)diphenhydramine will increase the level or effect of aripiprazole by affecting hepatic enzyme CYP2D6 metabolism.

Monitor Closely (1)diphenhydramine increases and armodafinil decreases sedation. Minor (1)ashwagandha increases effects of diphenhydramine by pharmacodynamic synergism.

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