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Loratadine Related Blood Catecholamines Decreased

Official FDA Reports0
Social Media Events3

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Claritin.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

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

Claritin Reditabs

... point of real pain, then ultimately an extreme lower backache (not experienced before Claritin); disrupted sleep (often by the pain mentioned above); suddenly lowered libido; vivid bizarre nightmares,...


Source:" CLARITIN: Side effects, ratings, and p...

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Did the author experience blood catecholamines decreased while taking claritin reditabs?

What is this?

Claritin

... almost impossible, even using tampons was unpleasant), really bad mood swings and irritability (especially during PMS time, which has never been a problem for me before), lower libido , and a drastic d...


Source:" CLARITIN-D 24 HOUR: Side effects, rati...

View full report on drug related blood catecholamines decreased

Did the author experience blood catecholamines decreased while taking claritin?

What is this?

Claritin

... me want to sleep, but sleep has been horrible--sweaty and restless. Body aches all over, especially back, shoulder, elbow, knee. Heart racing, inability to focus on anything, lower libido . I'm gla...


Source:" CLARITIN: Side effects, ratings, and p...

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Tell us about your Experience with Loratadine Related Blood Catecholamines Decreased

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Druginformer Identified Side Effects: Arthralgia, Back pain, Fatigue, Pain, Paranoia, Nightmare, Blood catecholamines decreased, Apathy, Depression, Hypertension, Insomnia, Irritability, Psychomotor hyperactivity, Irregular sleep phase

Posted By Anonymous in askapatient.com on September 11, 2015 @ 12:00 am

Hyperactive, racing mind and attention deficit, in that it was hard to focus on any task for long (ADHD?); increasingly aching joints to the point of real pain, then ultimately an extrem...

Druginformer Identified Side Effects: Fatigue, Vulvovaginal dryness, Mood swings, Blood catecholamines decreased, Irritability, Mood altered

Posted By Anonymous in askapatient.com on July 10, 2012 @ 12:00 am

... muscle strength despite working out intensely my entire life). Now that I've stopped taking it for a couple weeks, these things are beginning to subside, but now I'm horribly exhausted all day every d...

Druginformer Identified Side Effects: Arthralgia, Fatigue, Anxiety, Cardiac flutter, Blood catecholamines decreased, Disturbance in attention, Restlessness, Fear

Posted By Anonymous in askapatient.com on June 8, 2007 @ 12:00 am

Side Effects: Extreme anxiety. A constant feeling of impending doom. Makes me want to sleep, but sleep has been horrible--sweaty and restless. Body aches all over, especially back, shoulder, elbow...



* 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.