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Bicitra Side Effects

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Common Bicitra Side Effects


The most commonly reported Bicitra side effects (click to view or check a box to report):

Blood Potassium Increased (2)
Fibrosis (1)
Injury (1)
Joint Range Of Motion Decreased (1)
Fear (1)
Erythema (1)
Unevaluable Event (1)
Anxiety (1)
Depression (1)
Multi-organ Failure (1)
Nephrogenic Systemic Fibrosis (1)
Scar (1)
Skin Exfoliation (1)
Skin Hypertrophy (1)
Renal Injury (1)
Renal Failure (1)
Oedema Peripheral (1)
Pain (1)
Oedema (1)


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.

Bicitra Side Effects Reported to FDA


Bicitra Side Effect Report#8463484-8
Fibrosis, Skin Hypertrophy, Skin Exfoliation, Nephrogenic Systemic Fibrosis, Erythema, Oedema Peripheral, Scar, Joint Range Of Motion Decreased, Oedema
This is a report of a 58-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: NA, who was treated with Bicitra (dosage: NA, start time:
May 01, 2005), combined with:
  • Foltx (1 Tab Daily)
  • Plavix (75 Mg, Qd)
  • Dexamethasone
  • Acetaminophen (650 Mg, 2 Tabs Prn)
  • Adriamycin Pfs (15.7 Mg, In 250 Ml Nomral Saline Infuse Over 24 Hr Daily)
  • Compazine (10 Mg, Q6hr Prn)
  • Dilaudid
  • Magnevist (Unk)
and developed a serious reaction and side effect(s): Fibrosis, Skin Hypertrophy, Skin Exfoliation, Nephrogenic Systemic Fibrosis, Erythema, Oedema Peripheral, Scar, Joint Range Of Motion Decreased, Oedema after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Bicitra treatment in female patients, resulting in Fibrosis side effect.
Bicitra Side Effect Report#7386911-6
Fear, Depression, Renal Failure, Pain, Injury, Renal Injury, Unevaluable Event, Multi-organ Failure, Anxiety
This report suggests a potential Bicitra Fear side effect(s) that can have serious consequences. A female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: renal failure,gastrooesophageal reflux disease and used Bicitra (dosage: 3 Ml Every 12 Hrs) starting
Dec 02, 2005. After starting Bicitra the patient began experiencing various side effects, including: Fear, Depression, Renal Failure, Pain, Injury, Renal Injury, Unevaluable Event, Multi-organ Failure, AnxietyAdditional drugs used concurrently:
  • Reglan (0.3 Mg Every 12 Hrs)
  • Platelets (55 Ml)
  • Omnipaque 140 (54cc)
  • Trasylol,trasylol (1 Ml, Unk)
  • Red Blood Cells (1 Unit)
  • Red Blood Cells
  • Levothyroxine Sodium (0.25 Mg, Qd)
  • Zantac (7.5 Mg Every 12 Hrs)
Although Bicitra demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Fear, may still occur.
Bicitra Side Effect Report#5429524-5
Blood Potassium Increased
This Blood Potassium Increased problem was reported by a pharmacist from United States. A 37-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Bicitra (dosage: NA). The following drugs were being taken at the same time:
  • Polycitra
When using Bicitra, the patient experienced the following unwanted symptoms/side effects: Blood Potassium IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Potassium Increased, may become evident only after a product is in use by the general population.
Bicitra Side Effect Report#5425127-7
Blood Potassium Increased
This Blood Potassium Increased side effect was reported by a pharmacist from United States. A 37-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Bicitra (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Polycitra
.After starting to take Bicitra the consumer reported adverse symptoms, such as: Blood Potassium IncreasedThese side effects may potentially be related to Bicitra.



The appearance of Bicitra 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 Bicitra Side Effects for Men?

Men Side EffectsReports

Track Your Side Effects

Note Your Observations

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

  • Log Form

    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:
    Side Effects Scale 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.

    Bicitra 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.

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    Bicitra Safety Alerts, Active Ingredients, Usage Information

    More About Bicitra

    Side Effects reported to FDA: 4

    Bicitra safety alerts: No

    Latest Bicitra clinical trials