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User Voices for Nortriptyline Hydrochloride

The following are comments from users that experienced side effects while taking Nortriptyline Hydrochloride

Sleep Terror

Side Effects: I tried at bedtime and couldn't sleep at all. Then I started taking it in the daytime and had pain relief with Effexor added. terrible nightmares and sweating. Six months passed and I s...


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Sleep Terror

Side Effects: My side Effects are Vivid Nightmares , dry mouth, weight gain. Loss of sexual appetite.

I used to receive 3 migraines in a week. Prevented me from living a life. work was effe...


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Sleep Terror

... more painful than usual. My Dr. increased from 20 to 30mg and also said it takes about a month to really kick in. I have also noticed dark urine and have some very vivid nightmares that affect my sl...


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Sleep Terror

... extreme mood swings, one second I'm fine the next I'm crying the next I'm angry the next I'm laughing, dry mouth, chills, excessive sweat, weird scary and vivid nightmares , terrible nausea, vomiting, ...


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Sleep Terror

Side Effects: Dry mouth, trouble sleeping, vivid and I mean vivid nightmares , constipation, lime a brain zapping feeling, weight gain of 10 pounds in one month, Constantly hungry, sweating like crazy...


Source: PAMELOR: Side effects, ratings, and pa...

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Sleep Terror

... Cymbalta did not seemed to b be working anymore but after taking this medicine I experienced hand swelling, hallucinations, sleeping for about 15 hours and had terrible nightmares . Gained about 5 lb...


Source: Pamelor Oral : User Ratings covering u...

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* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.