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Parapres Side Effects

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Common Parapres Side Effects


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

Renal Failure (3)
Hyperkalaemia (3)
Renal Failure Acute (3)
Atrioventricular Block Complete (2)
Bradycardia (2)
Hyponatraemia (2)
Nodal Rhythm (1)
Atrial Fibrillation (1)
Autoimmune Thrombocytopenia (1)
Hyperhidrosis (1)
Asthenia (1)
Hypokalaemia (1)
Hypotension (1)
Toxicity To Various Agents (1)
Abdominal Pain (1)
Angioedema (1)
Oedema Peripheral (1)
Status Epilepticus (1)
Renal Tubular Necrosis (1)
Eczema Asteatotic (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.

Parapres Side Effects Reported to FDA



Parapres Side Effect Report#9704836
Renal Tubular Necrosis
This is a report of a 93-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: hypertension,pain,urinary tract infection, who was treated with Parapres Plus (dosage: 16 Mg/12.5 Mg 1 Df, Every Day, start time: 201301), combined with:
  • Paracetamol
  • Augmentine (875 Mg/125 Mg)
  • Fosfomycin
  • Zolpidem
  • Cromatonbic B12 1000 Inyectable, 8 Ampollas De 1 Ml (Ampoules Of 1 Ml, 1 Bottle To Drink)
  • Venlafaxina
  • Simvastatina
  • Adiro 100 Mg Comprimidos Gastrorresistentes Efg 30 Comprimidos
and developed a serious reaction and side effect(s): Renal Tubular Necrosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Parapres Plus treatment in female patients, resulting in Renal Tubular Necrosis side effect. The patient was hospitalized.
Parapres Side Effect Report#9643660
Status Epilepticus, Hyponatraemia
This report suggests a potential Parapres Plus Status Epilepticus side effect(s) that can have serious consequences. A 78-year-old female patient (weight: NA) from ES was diagnosed with the following symptoms/conditions: hypertension,constipation,colonoscopy,incontinence,hypothyroidism,hypovitaminosis,osteoporosis and used Parapres Plus (dosage: 32 Mg/ 12.5 Mg, 1df Every Day) starting
Sep 20, 2010. After starting Parapres Plus the patient began experiencing various side effects, including: Status Epilepticus, HyponatraemiaAdditional drugs used concurrently:
  • Plantaben (1 Or 2 Sachets)
  • Citrafleet Polvo Para (1 Or 2 Sachets, Frequency Not Provided)
  • Toviaz
  • Eutirox
  • Natecal D
  • Actonel Semanal
The patient was hospitalized. Although Parapres Plus demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Status Epilepticus, may still occur.
Parapres Side Effect Report#9285974
Abdominal Pain, Hepatitis Cholestatic
This Abdominal Pain problem was reported by a physician from ES. A 74-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 17, 2012 this consumer started treatment with Parapres Plus (dosage: Candesartan Cilexetil 16 Mg/hydrochlorothiazide 12.5 Mg). The following drugs were being taken at the same time:
  • Omeprazol
  • Roname
  • Vytorin (10 Mg/20 Mg)
  • Trajenta
  • Celebrex
  • Adiro
  • Nolotil (575 Mg As Needed)
  • Plantago Ovata Leaf
When using Parapres Plus, the patient experienced the following unwanted symptoms/side effects: Abdominal Pain, Hepatitis CholestaticThe 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 Abdominal Pain, may become evident only after a product is in use by the general population.
Parapres Side Effect Report#9121305
Nodal Rhythm, Toxicity To Various Agents
This Nodal Rhythm side effect was reported by a physician from ES. A 79-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Parapres Plus (drug dosage: Candesartan Cilexetil 16 Mg/hydrochlorothiazide 12.5 Mg (1 D)), which was initiated on 2010. Concurrently used drugs:
  • Atenolol
  • Digoxina
  • Aldactone
  • Furosemida
  • Levothroid
.After starting to take Parapres Plus the consumer reported adverse symptoms, such as: Nodal Rhythm, Toxicity To Various AgentsThese side effects may potentially be related to Parapres Plus. The patient was hospitalized.
Parapres Side Effect Report#8842453
Cerebrovascular Accident, Atrioventricular Block Complete, Atrial Fibrillation, Hyperkalaemia
This is a report of a 84-year-old female patient (weight: NA) from JP, suffering from the following health symptoms/conditions: hypertension,gout, who was treated with Parapres (dosage: NA, start time: 2005), combined with:
  • Colchicine
  • Allopurinol
  • Adiro
  • Seguril
  • Astudal
and developed a serious reaction and side effect(s): Cerebrovascular Accident, Atrioventricular Block Complete, Atrial Fibrillation, Hyperkalaemia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Parapres treatment in female patients, resulting in Cerebrovascular Accident side effect. The patient was hospitalized.
Parapres Side Effect Report#7392566-7
Renal Failure Acute
This report suggests a potential Parapres Comprimidos Renal Failure Acute side effect(s) that can have serious consequences. A 62-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: hypertension and used Parapres Comprimidos (dosage: NA) starting
Mar 01, 2008. After starting Parapres Comprimidos the patient began experiencing various side effects, including: Renal Failure AcuteAdditional drugs used concurrently:
  • Esertia
  • Seguril
  • Coropres
  • Allopurinol
  • Norvasc
The patient was hospitalized. Although Parapres Comprimidos demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Renal Failure Acute, may still occur.
Parapres Side Effect Report#7130551-0
Autoimmune Thrombocytopenia
This Autoimmune Thrombocytopenia problem was reported by a physician from Japan. A 52-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Jan 01, 2004 this consumer started treatment with Parapres 4 Mg Comprimidos (dosage: NA). The following drugs were being taken at the same time: NA. When using Parapres 4 Mg Comprimidos, the patient experienced the following unwanted symptoms/side effects: Autoimmune ThrombocytopeniaThe 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 Autoimmune Thrombocytopenia, may become evident only after a product is in use by the general population.
Parapres Side Effect Report#6688227-X
Renal Failure Acute
This Renal Failure Acute side effect was reported by a health professional from Japan. A 95-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Parapres Plus (drug dosage: 16/12.5 Mg; 1 Df Daily), which was initiated on
Jan 01, 2009. Concurrently used drugs:
  • Furosemide
  • Amaryl
  • Aspirin
  • Natecal D
.After starting to take Parapres Plus the consumer reported adverse symptoms, such as: Renal Failure AcuteThese side effects may potentially be related to Parapres Plus. The patient was hospitalized.
Parapres Side Effect Report#6673221-5
Renal Failure Acute
This is a report of a 95-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: hypertension, who was treated with Parapres Plus (dosage: 16/12.5 Mg; 1 Df Daily, start time:
Jan 01, 2009), combined with:
  • Furosemide
  • Amaryl
  • Aspirin
  • Natecal D
and developed a serious reaction and side effect(s): Renal Failure Acute after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Parapres Plus treatment in female patients, resulting in Renal Failure Acute side effect. The patient was hospitalized.
Parapres Side Effect Report#6554037-7
Atrioventricular Block Complete, Cardiogenic Shock, Hyperkalaemia
This report suggests a potential Parapres Atrioventricular Block Complete side effect(s) that can have serious consequences. A 92-year-old female patient (weight: NA) from Spain was diagnosed with the following symptoms/conditions: hypertension and used Parapres (dosage: NA) starting
Jan 01, 2006. After starting Parapres the patient began experiencing various side effects, including: Atrioventricular Block Complete, Cardiogenic Shock, HyperkalaemiaAdditional drugs used concurrently:
  • Aldactone
  • Omeprazol
  • Seguril
  • Sintrom
  • Zocor
The patient was hospitalized. Although Parapres demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Atrioventricular Block Complete, may still occur.
Parapres Side Effect Report#6403559-8
Bradycardia, Hyperkalaemia
This Bradycardia problem was reported by a health professional from Japan. A 80-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2001 this consumer started treatment with Parapres (dosage: NA). The following drugs were being taken at the same time: NA. When using Parapres, the patient experienced the following unwanted symptoms/side effects: Bradycardia, HyperkalaemiaThe 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 Bradycardia, may become evident only after a product is in use by the general population.
Parapres Side Effect Report#6156895-7
Angioedema, Eczema Asteatotic, Eosinophilia, Oedema Peripheral, Renal Failure
This Angioedema side effect was reported by a health professional from Japan. A 76-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Parapres (drug dosage: NA), which was initiated on
Feb 10, 2009. Concurrently used drugs: NA..After starting to take Parapres the consumer reported adverse symptoms, such as: Angioedema, Eczema Asteatotic, Eosinophilia, Oedema Peripheral, Renal FailureThese side effects may potentially be related to Parapres. The patient was hospitalized.
Parapres Side Effect Report#6107653-0
Blood Creatinine Increased, Blood Urea Increased, Renal Failure
This is a report of a 46-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: hypertension, who was treated with Parapres (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Blood Creatinine Increased, Blood Urea Increased, Renal Failure after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Parapres treatment in female patients, resulting in Blood Creatinine Increased side effect. The patient was hospitalized.
Parapres Side Effect Report#6081716-0
Asthenia, Confusional State, Renal Failure
This report suggests a potential Parapres Asthenia side effect(s) that can have serious consequences. A 83-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: cardiac failure and used Parapres (dosage: NA) starting
Sep 28, 2008. After starting Parapres the patient began experiencing various side effects, including: Asthenia, Confusional State, Renal FailureAdditional drugs used concurrently:
  • Furosemide
  • Sintrom
  • Digitalis Tab
  • Espironolacton
Although Parapres demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Asthenia, may still occur.
Parapres Side Effect Report#5924255-7
Hyponatraemia
This Hyponatraemia problem was reported by a health professional from Japan. A 68-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Sep 01, 2008 this consumer started treatment with Parapres 16 Mg Comprimidos, 28 Comprimidos (dosage: NA). The following drugs were being taken at the same time:
  • Seguril 40 Mg Comprimidos, 10 Comprimidos
  • Aldactone
  • Oxcarbazepine
  • Sintrom Uno Geigy 1mg 60 Comprimidos
  • Boi-k , 20 Comprimidos
When using Parapres 16 Mg Comprimidos, 28 Comprimidos, the patient experienced the following unwanted symptoms/side effects: HyponatraemiaThe 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 Hyponatraemia, may become evident only after a product is in use by the general population.
Parapres Side Effect Report#5501814-7
Bone Marrow Failure
This Bone Marrow Failure side effect was reported by a health professional from Spain. A 78-year-old male patient (weight:NA) experienced the following symptoms/conditions: hypertension,hyperuricaemia,gastrooesophageal reflux disease,gout,ischaemia.The patient was prescribed Parapres (drug dosage: NA), which was initiated on
Feb 01, 2001. Concurrently used drugs:
  • Zyloric
  • Pantoprazol
  • Colchicine Houde
  • Hemovas
.After starting to take Parapres the consumer reported adverse symptoms, such as: Bone Marrow FailureThese side effects may potentially be related to Parapres. The patient was hospitalized.
Parapres Side Effect Report#4708122-2
Bradycardia, Dizziness, Hyperhidrosis, Hypokalaemia, Hypotension
This is a report of a 56-year-old male patient (weight: NA) from Spain, suffering from the following health symptoms/conditions: essential hypertension, who was treated with Parapres (dosage: NA, start time: NS), combined with:
  • Chlorthalidone
  • Montelukast Sodium
  • Symbicort Turbuhaler
and developed a serious reaction and side effect(s): Bradycardia, Dizziness, Hyperhidrosis, Hypokalaemia, Hypotension after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Parapres treatment in male patients, resulting in Bradycardia side effect. The patient was hospitalized.



The appearance of Parapres 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.

    Parapres 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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    More About Parapres

    Side Effects reported to FDA: 17

    Parapres safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 7

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