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.
and developed a serious reaction and side effect(s): Respiratory Tract Infection Bacterial, Electrocardiogram Qt Prolonged after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Ciprofloxacina Ratiopharm 500 Mg treatment in female patients, resulting in Respiratory Tract Infection Bacterial side effect.
This report suggests a potential Ciprofloxacina 500 Mg RatiopharmTendonitis side effect(s) that can have serious consequences. A 49-year-old male patient (weight: NA) from PT was diagnosed with the following symptoms/conditions: prostatitis,asthma and used Ciprofloxacina 500 Mg Ratiopharm (dosage: 500 Milligram Daily; 1) starting 2007. After starting Ciprofloxacina 500 Mg Ratiopharm the patient began experiencing various side effects, including: Tendonitis, Paraesthesia, Gait Disturbance, Erectile Dysfunction, Muscle Rigidity, Arthralgia, Burning Sensation, Muscle Atrophy, Muscle Contractions InvoluntaryAdditional drugs used concurrently:
Although Ciprofloxacina 500 Mg Ratiopharm demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Tendonitis, may still occur.
Ciprofloxacina Side Effect Report#5521716-X Arthralgia, Erythema, Gait Disturbance, Myalgia, Pain In Extremity
This Arthralgia problem was reported by a pharmacist from Germany. A 69-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: urinary tract infection,hypertension. On
Jan 01, 2006 this consumer started treatment with Ciprofloxacina (dosage: 1 G/day). The following drugs were being taken at the same time:
Lopressor (100 Mg/day)
When using Ciprofloxacina, the patient experienced the following unwanted symptoms/side effects: Arthralgia, Erythema, Gait Disturbance, Myalgia, Pain In ExtremityAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Arthralgia, may become evident only after a product is in use by the general population.
The appearance of Ciprofloxacina 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.
What are common Ciprofloxacina Side Effects for Women?
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.
Ciprofloxacina 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.