HappeningToo topic
Acyclovir reports
Browse community reports connected to Acyclovir. These reports can show that other people are describing similar experiences, but they do not prove that Acyclovir caused a symptom or reaction.
⚕️ Medicine safety note
Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.
38 problems
Abdominal Discomfort while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and abdominal discomfort appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain Upper while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and abdominal pain upper appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and abdominal pain appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Alopecia while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and alopecia appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Anxiety while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and anxiety appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Back Pain while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and back pain appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Chills while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and chills appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Constipation while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and constipation appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Cough while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and cough appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Decreased Appetite while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and decreased appetite appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dehydration while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and dehydration appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Diarrhea while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and diarrhea appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dizziness while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and dizziness appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Fatigue while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and fatigue appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Feeling Abnormal while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and feeling abnormal appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Headache while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and headache appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hives while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and hives appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hypotension while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and hypotension appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Insomnia while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and insomnia appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Itching while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and itching appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Malaise while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and malaise appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Muscle Spasms while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and muscle spasms appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Muscular Weakness while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and muscular weakness appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Myalgia while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and myalgia appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nausea while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and nausea appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Pain while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and pain appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Peripheral swelling while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and peripheral swelling appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Rash while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and rash appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Shortness of breath while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and shortness of breath appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Skin redness while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and skin redness appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Sleepiness while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and sleepiness appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tingling or pins and needles while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and tingling or pins and needles appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tremor while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and tremor appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vision Blurred while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and vision blurred appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vomiting while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and vomiting appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weakness while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and weakness appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Decreased while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and weight decreased appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Increased while using Acyclovir
FDA FAERS contains adverse-event reports in which Acyclovir and weight increased appear together. This does not establish that Acyclovir caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →