The risk of administering methylene blue by non-intravenous routes such as oral tablets or by local injection or in intravenous doses much lower than 1 mg kg with remeron is unclear.
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Other Adverse Events Observed During The Premarketing Evaluation Of REMERON.
Report any new or worsening symptoms to your doctorsuch asmood or behavior changesanxietypanic attackstrouble sleepingor if you feel impulsiveirritableagitatedhostileaggressiverestlesshyperactivementally or physicallymore depressedor have thoughts about suicide or hurting yourself.
9Severe skin reactionsCall your doctor right away if you have any or all of the following symptoms:
Do not stop using Remeron suddenlyor you could have unpleasant withdrawal symptomsAsk your doctor how to safely stop using mirtazapine.
Before you take REMERONtell your healthcare provider about all of your medical conditionsincluding if you:
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