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Trivastal Side Effects

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Common Trivastal Side Effects


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

C-reactive Protein Increased (2)
Eye Pain (2)
Overdose (1)
Pseudomonas Infection (1)
Orthostatic Hypotension (1)
Rhabdomyolysis (1)
Sinus Tachycardia (1)
Glaucoma (1)
Haematoma (1)
Treatment Failure (1)
Ocular Hypertension (1)
Mechanical Ventilation Complication (1)
Leukocytosis (1)
Loss Of Consciousness (1)
Malaise (1)
Jugular Vein Distension (1)
Inflammation (1)
Haemoglobin Decreased (1)
Hallucination (1)
Normochromic Normocytic Anaemia (1)

➢ More



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.

Trivastal Side Effects Reported to FDA



Trivastal Side Effect Report#8213489-7
Completed Suicide
This is a report of a 69-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Trivastal (dosage: NA, start time:
Jan 01, 2009), combined with:
  • Sinemet Cr
  • Comtan
  • Sinemet
and developed a serious reaction and side effect(s): Completed Suicide after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Trivastal treatment in female patients, resulting in Completed Suicide side effect.
Trivastal Side Effect Report#8047627-6
Normochromic Normocytic Anaemia, Overdose, Haematoma
This report suggests a potential Trivastal Normochromic Normocytic Anaemia side effect(s) that can have serious consequences. A female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Trivastal (dosage: NA) starting
Jul 05, 2011. After starting Trivastal the patient began experiencing various side effects, including: Normochromic Normocytic Anaemia, Overdose, HaematomaAdditional drugs used concurrently:
  • Acetaminophen
  • Arixtra (7.5mg Per Day)
  • Modopar
  • Nitroglycerin
  • Lorazepam
  • Diamicron
  • Zopiclone
The patient was hospitalized. Although Trivastal demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Normochromic Normocytic Anaemia, may still occur.
Trivastal Side Effect Report#7956930-7
Rhabdomyolysis, Fall, Urinary Retention
This Rhabdomyolysis problem was reported by a physician from France. A 90-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2007 this consumer started treatment with Trivastal (dosage: NA). The following drugs were being taken at the same time:
  • Hyzaar (3/4 Df)
  • Clonazepam
  • Clonazepam
  • Acetaminophen
  • Transulose
  • Clonazepam
  • Aspirin
  • Crestor
When using Trivastal, the patient experienced the following unwanted symptoms/side effects: Rhabdomyolysis, Fall, Urinary RetentionThe 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 Rhabdomyolysis, may become evident only after a product is in use by the general population.
Trivastal Side Effect Report#7323257-6
Pseudomonas Infection, C-reactive Protein Increased, Treatment Failure, Sinus Tachycardia, Haemoglobin Decreased, Acute Respiratory Distress Syndrome, Jugular Vein Distension, Mechanical Ventilation Complication, Inflammation
This Pseudomonas Infection side effect was reported by a physician from France. A 86-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Trivastal /00397201/ (piribedil) (drug dosage: NA), which was initiated on
Nov 01, 2010. Concurrently used drugs:
  • Furadantin (Oral)
  • Atacand
  • Kardegic /00002703/ (acetylsalicylate Lysine)
  • Movicol /01053601/ (macrogol, Potassium Chloride, Sodium Bicarbonate,
  • Donormyl /00334102/ (doxylamine Succinate)
  • Actonel
  • Calcit-s (calcitonin, Salmon)
  • Pantoprazole Sodium
.After starting to take Trivastal /00397201/ (piribedil) the consumer reported adverse symptoms, such as: Pseudomonas Infection, C-reactive Protein Increased, Treatment Failure, Sinus Tachycardia, Haemoglobin Decreased, Acute Respiratory Distress Syndrome, Jugular Vein Distension, Mechanical Ventilation Complication, InflammationThese side effects may potentially be related to Trivastal /00397201/ (piribedil). The patient was hospitalized.
Trivastal Side Effect Report#5291678-1
Abnormal Behaviour, Aggression, Conversion Disorder, Dementia, Disorientation, Hallucination
This is a report of a 81-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: parkinsonism, who was treated with Trivastal (dosage: 50 Mg, Bid, start time:
Dec 15, 2006), combined with:
  • Modopar (125 Mg, Qid)
  • Modopar (250 Mg, 5qd)
  • Requip
  • Cotareg (1 Df, Qd)
  • Trimetazidine
  • Zoloft (25 Mg, Qd)
  • Nisisco (1 Df, Qd)
and developed a serious reaction and side effect(s): Abnormal Behaviour, Aggression, Conversion Disorder, Dementia, Disorientation, Hallucination after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Trivastal treatment in female patients, resulting in Abnormal Behaviour side effect. The patient was hospitalized.
Trivastal Side Effect Report#5106768-3
Eye Pain, Ocular Hypertension
This report suggests a potential Trivastal Eye Pain side effect(s) that can have serious consequences. A 77-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Trivastal (dosage: 150 Mg Daily) starting
Apr 01, 2004. After starting Trivastal the patient began experiencing various side effects, including: Eye Pain, Ocular HypertensionAdditional drugs used concurrently:
  • Deprenyl (5 Mg, Qd)
  • Stalevo 100 (800/600/150 Mg Daily)
  • Modopar (25/100 To 50/200 Mg Daily)
Although Trivastal demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eye Pain, may still occur.
Trivastal Side Effect Report#5103231-0
Anorexia, Bacteraemia, Bacteriuria, Bladder Catheterisation, C-reactive Protein Increased, Creatinine Renal Clearance Decreased, Diarrhoea, Fluid Replacement
This Anorexia problem was reported by a consumer or non-health professional from France. A 80-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Trivastal (dosage: NA). The following drugs were being taken at the same time:
  • Sinemet (4 Df Daily)
  • Stablon
  • Comtan
When using Trivastal, the patient experienced the following unwanted symptoms/side effects: Anorexia, Bacteraemia, Bacteriuria, Bladder Catheterisation, C-reactive Protein Increased, Creatinine Renal Clearance Decreased, Diarrhoea, Fluid ReplacementThe 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 Anorexia, may become evident only after a product is in use by the general population.
Trivastal Side Effect Report#5023083-7
Eye Pain, Glaucoma
This Eye Pain side effect was reported by a physician from France. A 77-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Trivastal (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Deprenyl
  • Stalevo 100
.After starting to take Trivastal the consumer reported adverse symptoms, such as: Eye Pain, GlaucomaThese side effects may potentially be related to Trivastal.
Trivastal Side Effect Report#4553051-0
Blood Pressure Orthostatic Decreased, Leukocytosis, Loss Of Consciousness, Malaise, Orthostatic Hypotension
This is a report of a 84-year-old female patient (weight: NA) from , suffering from the following health symptoms/conditions: essential hypertension, who was treated with Trivastal (dosage: 50 Mg, Tid, start time: NS), combined with:
  • Lasilix (20 Mg, Qd)
  • Risperdal (Unk, Unk)
  • Nitriderm Tts (5 Mg/24hrs)
  • Cordarone (Unk, Unk)
  • Nisis (1 Df, Qd)
and developed a serious reaction and side effect(s): Blood Pressure Orthostatic Decreased, Leukocytosis, Loss Of Consciousness, Malaise, Orthostatic Hypotension after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Trivastal treatment in female patients, resulting in Blood Pressure Orthostatic Decreased side effect. The patient was hospitalized.



The appearance of Trivastal 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.

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.

    Trivastal 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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    Trivastal Safety Alerts, Active Ingredients, Usage Information

    More About Trivastal

    Side Effects reported to FDA: 9

    Trivastal safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 5

    Latest Trivastal clinical trials