If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.
Livial Side Effects Reported to FDA
Livial Side Effect Report#8241327-5 Cervix Carcinoma Stage Ii, Disease Progression
This is a report of a 58-year-old female patient (weight: NA) from Sweden, suffering from the following health symptoms/conditions: NA, who was treated with Livial (dosage: NA, start time:
Nov 10, 2000), combined with:
Enalapril Maleate (2.5 Mgx1)
Somatropin (0.30 Mg, 1x/day)
and developed a serious reaction and side effect(s): Cervix Carcinoma Stage Ii, Disease Progression after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Livial treatment in female patients, resulting in Cervix Carcinoma Stage Ii side effect. The patient was hospitalized.
Livial Side Effect Report#7573987-6 Renal Cyst, Skin Disorder, Acne, Rash
This report suggests a potential LivialRenal Cyst side effect(s) that can have serious consequences. A female patient (weight: NA) from Netherlands was diagnosed with the following symptoms/conditions: hot flush,endometriosis and used Livial (dosage: NA) starting
Feb 01, 2011. After starting Livial the patient began experiencing various side effects, including: Renal Cyst, Skin Disorder, Acne, RashAdditional drugs used concurrently:
Although Livial demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Renal Cyst, may still occur.
Livial Side Effect Report#7428980-0 Hepatic Pain, Hepatitis
This Hepatic Pain problem was reported by a consumer or non-health professional from Mexico. A 60-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2001 this consumer started treatment with Livial (dosage: NA). The following drugs were being taken at the same time:
Actonel (35 Mg, Once A Week, Oral)
When using Livial, the patient experienced the following unwanted symptoms/side effects: Hepatic Pain, HepatitisThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Hepatic Pain, may become evident only after a product is in use by the general population.
This Eye Irritation side effect was reported by a consumer or non-health professional from Netherlands. A patient (weight:NA) experienced the following symptoms/conditions: hot flush,leiomyoma,prophylaxis,uterine enlargement.The patient was prescribed Livial (drug dosage: NA), which was initiated on
Jul 12, 2010. Concurrently used drugs:
.After starting to take Livial the consumer reported adverse symptoms, such as: Eye Irritation, Arthropathy, Hair Disorder, Hysterectomy, Fatigue, DepressionThese side effects may potentially be related to Livial. The patient was hospitalized.
The appearance of Livial on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.
It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.
Why Your Notes are Important
Your notes could be helpful in several ways:
You can use them to remind you of details that may alert your health care professional(s) to a problem
You will have a record to refer to in the future, in case you are ever prescribed the same medicine again
You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.
Medicine Name and Dosage:
Date & Time
Other Medicine(s) or Treatment(s)
Scale: 1 = very mild to 10 = very bad
Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Livial reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.