* Druginformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an official signal from the FDA or other regulatory entity.
Valsartan Adverse Event Reports (From Social Media - User Reviews and Forum Discussions)
... in hunger. Substantial. Not just an urge to eat but hungry to the point of discomfort. I tried eating carrots and celery, drinking lots of water and milk, but still I gained weight . I also lost vi...
... to take it, not getting RX refilled in time, chaning RX's, going back to Diovan, etc., my side effects became more noticeable and I had more of them. Moderate to sever muscle aches were my major side...
... back to Diovan, etc., my side effects became more noticeable and I had more of them. Moderate to sever muscle aches were my major side effect. Noticed more concentration required during driving, and...
Side Effects: Initially I didn't notice any side effects. After time, sometimes forgetting to take it, not getting RX refilled in time, chaning RX's, going back to Diovan, etc., my side effects beca...
... dosage was upped to 160 mg. Noticed more side effects on that dosage than on the 80 mg dose. Also caffeine seems to play a major role for me in rising bp, as well as salt causing water retention ....
... and I had more of them. Moderate to sever muscle aches were my major side effect. Noticed more concentration required during driving, and eye vision blurriness .
... blood pressure. If I was consistent with my dosage, after time if I missed a dose it wouldn't matter. If I was inconsistent and forgetful with my dosage, I could feel heart palpitations and my bp wo...
... rash with HC Derma-Pax and applied Hydrocortisone Cream afterward. Continued med and random daily BP reading to advise cardiologist if BP altered by increased dosage. If hives recur, will call Dr. and...
* 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 AERS: The Adverse Event Reporting System (AERS) 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 AERS. The AERS 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, AERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.
The total number of adverse event reports in the FDA-owned Adverse Event Reporting System (AERS).
The total number of adverse event reports extracted from online social media sources (forum discussions, user reviews, etc).
The total number of distinct comments (forum posts, user reviews, etc) written by users of a drug.