This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Adcirca.
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.
Report Date | Dosage | Indication | Outcome | Country | Gender | Age | Weight (lbs) |
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* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.
Druginformer Identified Side Effects: Back pain, Headache, Dizziness, Nausea, Pain, Anxiety, Visual impairment, Drug ineffective, Hyperhidrosis, Joint stiffness, Vision blurred
Posted By Anonymous in askapatient.com on October 27, 2011 @ 12:00 am
“... headache began. The last five days have been hell. I'm 61 years old and have never been sicker. Finally, vision is beginning to clear (though still slightly blurred), pain in back, legs and buttocks a...”
Druginformer Identified Side Effects: Eructation, Headache, Feeling cold, Dizziness, Muscle strain, Dyspepsia, Hyperhidrosis, Tenderness
Posted By Anonymous in askapatient.com on April 11, 2008 @ 12:00 am
“Side Effects: Tried 20mg for the first time. Frequent belching and extreme heartburn started within the first couple of hours and made my mouth taste sour. I had a mild lingering headache after about...”
* 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.
Social Media Comments From Around the Web
The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride
Cialis
“Side Effects: After 2 1/2 months of taking cialis , vision began blurring in left eye and began developing mild pain and stiffness in lower neck and upper back. About 10 days later I had a stroke like...”
Source:" CIALIS: Side effects, ratings, and pat...
View full report on drug related hyperhidrosis
Did the author experience hyperhidrosis while taking cialis?
What is this?Cialis
“... I got up the next morning I had a huge charlie horse in the back of my leg. I became extremely dizzy and had to lay back down. I couldn't feel my pulse, got really cold and sweaty and thought I was go...”
Source:" CIALIS: Side effects, ratings, and pat...
View full report on drug related hyperhidrosis
Did the author experience hyperhidrosis while taking cialis?
What is this?