PatientsVille.com Logo

Apranax Side Effects

PatientsVille

Common Apranax Side Effects


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

Renal Failure Acute (9)
Histiocytosis Haematophagic (6)
Anaemia (5)
Alanine Aminotransferase Increased (4)
Aspartate Aminotransferase Increased (4)
C-reactive Protein Increased (4)
Enterocolitis Infectious (4)
Dyspnoea (4)
Gamma-glutamyltransferase Increased (3)
Blood Alkaline Phosphatase Increased (3)
Haemodialysis (3)
Pyrexia (3)
Inflammation (3)
Renal Failure (3)
Intra-uterine Death (3)
Metabolic Acidosis (2)
Melaena (2)
Loss Of Consciousness (2)
Lung Disorder (2)
Malaise (2)

➢ 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.

Apranax Side Effects Reported to FDA



Apranax Side Effect Report#9918843
Rash Maculo-papular
This is a report of a 49-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: neck pain, who was treated with Apranax (dosage: NA, start time:
Nov 12, 2013), combined with:
  • Vaxigrip
  • Pariet
  • Miorel (france)
and developed a serious reaction and side effect(s): Rash Maculo-papular after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in female patients, resulting in Rash Maculo-papular side effect. The patient was hospitalized.
Apranax Side Effect Report#9904187
Renal Colic, Nephrolithiasis
This report suggests a potential Apranax Renal Colic side effect(s) that can have serious consequences. A 14-year-old female patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: juvenile idiopathic arthritis and used Apranax (dosage: NA) starting 201002. After starting Apranax the patient began experiencing various side effects, including: Renal Colic, NephrolithiasisAdditional drugs used concurrently:
  • Humira
  • Humira (24 Mg/m2)
  • Humira
  • Methotrexate
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Renal Colic, may still occur.
Apranax Side Effect Report#9781274
Vulvovaginal Pruritus, Burning Sensation, Genital Lesion
This Vulvovaginal Pruritus problem was reported by a physician from FR. A 45-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: arthralgia. On
Oct 07, 2013 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time:
  • Voltarene (france)
  • Omeprazole
When using Apranax, the patient experienced the following unwanted symptoms/side effects: Vulvovaginal Pruritus, Burning Sensation, Genital LesionThe 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 Vulvovaginal Pruritus, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#9752217
Melaena, Confusional State, Renal Impairment, Hepatic Function Abnormal
This Melaena side effect was reported by a physician from FR. A 89-year-old female patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Apranax (drug dosage: 550 Mg), which was initiated on
Nov 12, 2013. Concurrently used drugs:
  • Tahor
  • Allopurinol
.After starting to take Apranax the consumer reported adverse symptoms, such as: Melaena, Confusional State, Renal Impairment, Hepatic Function AbnormalThese side effects may potentially be related to Apranax. The patient was hospitalized.
Apranax Side Effect Report#9706617
Hepatitis
This is a report of a 77-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: arthralgia,oedema peripheral, who was treated with Apranax (dosage: NA, start time:
Mar 26, 2013), combined with:
  • Aldactone (france)
  • Dafalgan Codeine
  • Dynamisan (france)
  • Burinex
  • Remicade
and developed a serious reaction and side effect(s): Hepatitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in female patients, resulting in Hepatitis side effect. The patient was hospitalized.
Apranax Side Effect Report#9595045
Lactic Acidosis, Renal Failure Acute
This report suggests a potential Apranax Lactic Acidosis side effect(s) that can have serious consequences. A 84-year-old male patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: NA and used Apranax (dosage: NA) starting NS. After starting Apranax the patient began experiencing various side effects, including: Lactic Acidosis, Renal Failure AcuteAdditional drugs used concurrently:
  • Stagid
  • Kardegic
  • Zaldiar
  • Lipanthyl
  • Lodoz (10/6.25 Mg)
  • Diamicron (60 Mg)
  • Alteis
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Lactic Acidosis, may still occur.
Apranax Side Effect Report#9525462
Renal Failure Acute, Tubulointerstitial Nephritis
This Renal Failure Acute problem was reported by a physician from FR. A 82-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Apr 18, 2013 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time:
  • Previscan (france)
  • Bicarbonate De Sodium
  • Kayexalate
  • Coumadine
When using Apranax, the patient experienced the following unwanted symptoms/side effects: Renal Failure Acute, Tubulointerstitial NephritisThe 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 Renal Failure Acute, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#9520523
Renal Failure Acute
This Renal Failure Acute side effect was reported by a physician from FR. A 15-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Apranax (drug dosage: 500 Mg In The Morning, 750 Mg In The Evening For 1 Month, Then 500 Mg Twice Daily), which was initiated on
Apr 11, 2013. Concurrently used drugs: NA..After starting to take Apranax the consumer reported adverse symptoms, such as: Renal Failure AcuteThese side effects may potentially be related to Apranax.
Apranax Side Effect Report#9474983
Acute Pulmonary Oedema, Hypertensive Crisis, Dyspnoea
This is a report of a 67-year-old male patient (weight: NA) from FR, suffering from the following health symptoms/conditions: arthralgia, who was treated with Apranax (dosage: 550 Mg, start time:
May 01, 2013), combined with:
  • Mopral (france) (20 Mg)
  • Vesicare
and developed a serious reaction and side effect(s): Acute Pulmonary Oedema, Hypertensive Crisis, Dyspnoea after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in male patients, resulting in Acute Pulmonary Oedema side effect. The patient was hospitalized.
Apranax Side Effect Report#9406485
Dermo-hypodermitis
This report suggests a potential Apranax Dermo-hypodermitis side effect(s) that can have serious consequences. A 53-year-old male patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: rheumatoid arthritis and used Apranax (dosage: 550 Mg) starting 2012. After starting Apranax the patient began experiencing various side effects, including: Dermo-hypodermitisAdditional drugs used concurrently:
  • Enbrel
  • Novatrex (2.5 Mg)
  • Feldene (Feldene Dispersible)
  • Profenid
  • Profenid
  • Ketoprofene
  • Miorel (france)
  • Ketum
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dermo-hypodermitis, may still occur.
Apranax Side Effect Report#9371163
Cellulitis
This Cellulitis problem was reported by a physician from FR. A 36-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: torticollis. On
Apr 17, 2013 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time:
  • Ibuprofene
When using Apranax, the patient experienced the following unwanted symptoms/side effects: CellulitisThe 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 Cellulitis, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#9330671
Histiocytosis Haematophagic
This Histiocytosis Haematophagic side effect was reported by a physician from FR. A 15-year-old female patient (weight:NA) experienced the following symptoms/conditions: juvenile idiopathic arthritis.The patient was prescribed Apranax (drug dosage: NA), which was initiated on 2010. Concurrently used drugs:
  • Methotrexate
  • Speciafoldine
  • Cortancyl
  • Solu-medrol
  • Kineret
.After starting to take Apranax the consumer reported adverse symptoms, such as: Histiocytosis HaematophagicThese side effects may potentially be related to Apranax. The patient was hospitalized.
Apranax Side Effect Report#9323046
Lung Disorder, Eosinophilia, Cholestasis
This is a report of a 60-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: musculoskeletal pain, who was treated with Apranax (dosage: NA, start time:
Apr 29, 2013), combined with:
  • Bilaska
and developed a serious reaction and side effect(s): Lung Disorder, Eosinophilia, Cholestasis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in female patients, resulting in Lung Disorder side effect. The patient was hospitalized.
Apranax Side Effect Report#9236720
Dermatitis Exfoliative, Eosinophilia, Pruritus
This report suggests a potential Apranax Dermatitis Exfoliative side effect(s) that can have serious consequences. A 47-year-old male patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: sciatica and used Apranax (dosage: NA) starting 2003. After starting Apranax the patient began experiencing various side effects, including: Dermatitis Exfoliative, Eosinophilia, PruritusAdditional drugs used concurrently:
  • Tegretol
  • Visipaque
  • Heparine Calcique
  • Medrol
  • Medrol
  • Medrol
  • Kenacort
  • Plaquenil
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dermatitis Exfoliative, may still occur.
Apranax Side Effect Report#9234218
Pulmonary Embolism, Phlebitis
This Pulmonary Embolism problem was reported by a physician from FR. A 44-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: ankylosing spondylitis. On
Mar 11, 2010 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time:
  • Simponi
  • Inexium
  • Topalgic Lp
  • Mirena
  • Skenan Lp
  • Actiskenan
When using Apranax, the patient experienced the following unwanted symptoms/side effects: Pulmonary Embolism, PhlebitisThe 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 Pulmonary Embolism, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#9197043
Haematoma, Shock Haemorrhagic
This Haematoma side effect was reported by a physician from FR. A 64-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Apranax (drug dosage: NA), which was initiated on
Feb 15, 2013. Concurrently used drugs:
  • Pradaxa
  • Deroxat
  • Inexium
.After starting to take Apranax the consumer reported adverse symptoms, such as: Haematoma, Shock HaemorrhagicThese side effects may potentially be related to Apranax.
Apranax Side Effect Report#9129426
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Thrombocytopenia, Anaemia, Renal Failure Acute
This is a report of a 54-year-old male patient (weight: NA) from FR, suffering from the following health symptoms/conditions: NA, who was treated with Apranax (dosage: NA, start time: NS), combined with:
  • Kardegic (1 Sachet)
  • Metoject
and developed a serious reaction and side effect(s): Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Thrombocytopenia, Anaemia, Renal Failure Acute after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in male patients, resulting in Alanine Aminotransferase Increased side effect. The patient was hospitalized.
Apranax Side Effect Report#8983889
Cholestasis, Jaundice
This report suggests a potential Apranax Cholestasis side effect(s) that can have serious consequences. A 53-year-old male patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: rheumatoid arthritis and used Apranax (dosage: NA) starting
Jan 23, 2012. After starting Apranax the patient began experiencing various side effects, including: Cholestasis, JaundiceAdditional drugs used concurrently:
  • Inexium
  • Arava
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cholestasis, may still occur.
Apranax Side Effect Report#8949807
Hepatitis Cholestatic
This Hepatitis Cholestatic problem was reported by a physician from FR. A 39-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jul 23, 2012 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time: NA. When using Apranax, the patient experienced the following unwanted symptoms/side effects: 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 Hepatitis Cholestatic, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#8877083
Melaena, Anaemia, Gastric Ulcer
This Melaena side effect was reported by a physician from FR. A 72-year-old female patient (weight:NA) experienced the following symptoms/conditions: osteoarthritis.The patient was prescribed Apranax (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Apranax the consumer reported adverse symptoms, such as: Melaena, Anaemia, Gastric UlcerThese side effects may potentially be related to Apranax. The patient was hospitalized.
Apranax Side Effect Report#8831990
Ileitis, Caecitis
This is a report of a female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: back pain, who was treated with Apranax (dosage: NA, start time:
Jul 22, 2012), combined with: NA. and developed a serious reaction and side effect(s): Ileitis, Caecitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in female patients, resulting in Ileitis side effect.
Apranax Side Effect Report#8812197
Gastritis Erosive
This report suggests a potential Apranax Gastritis Erosive side effect(s) that can have serious consequences. A 51-year-old male patient (weight: NA) from FR was diagnosed with the following symptoms/conditions: NA and used Apranax (dosage: NA) starting
Feb 22, 2012. After starting Apranax the patient began experiencing various side effects, including: Gastritis ErosiveAdditional drugs used concurrently:
  • Colchicine Opocalcium
  • Imodium
The patient was hospitalized. Although Apranax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Gastritis Erosive, may still occur.
Apranax Side Effect Report#8801656
Dermatitis Bullous, Paraesthesia, Inflammation, C-reactive Protein Increased, Erythema, Aphthous Stomatitis
This Dermatitis Bullous problem was reported by a health professional from FR. A 62-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: back pain. On
Feb 17, 2012 this consumer started treatment with Apranax (dosage: NA). The following drugs were being taken at the same time: NA. When using Apranax, the patient experienced the following unwanted symptoms/side effects: Dermatitis Bullous, Paraesthesia, Inflammation, C-reactive Protein Increased, Erythema, Aphthous StomatitisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dermatitis Bullous, may become evident only after a product is in use by the general population.
Apranax Side Effect Report#8794829
Enterocolitis Haemorrhagic, Rectal Haemorrhage
This Enterocolitis Haemorrhagic side effect was reported by a physician from FR. A 46-year-old male patient (weight:NA) experienced the following symptoms/conditions: back pain.The patient was prescribed Apranax (drug dosage: NA), which was initiated on
Aug 01, 2012. Concurrently used drugs:
  • Myolastan
  • Inexium
.After starting to take Apranax the consumer reported adverse symptoms, such as: Enterocolitis Haemorrhagic, Rectal HaemorrhageThese side effects may potentially be related to Apranax. The patient was hospitalized.
Apranax Side Effect Report#8641294
Neutropenia, Genital Ulceration
This is a report of a 57-year-old female patient (weight: NA) from FR, suffering from the following health symptoms/conditions: rheumatoid arthritis, who was treated with Apranax (dosage: NA, start time: 2002), combined with:
  • Methotrexat (Reported As Lmeth)
  • Enbrel
  • Lamaline
  • Speciafoldine
and developed a serious reaction and side effect(s): Neutropenia, Genital Ulceration after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Apranax treatment in female patients, resulting in Neutropenia side effect. The patient was hospitalized.


1 of 3 


The appearance of Apranax 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.

    Apranax 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.

    Discuss Apranax Side Effects

    Did You Have a Apranax Side Effect?

    Yes, Severe
    Yes, Moderate
    Yes, Minor
    No

    How Effective is Apranax for You?

    Exceeded Expectations
    Effective
    Somewhat Effective
    Not Effective

    Apranax Safety Alerts, Active Ingredients, Usage Information

    More About Apranax

    Side Effects reported to FDA: 68

    Apranax safety alerts: No

    Reported deaths: 9

    Reported hospitalizations: 46

    Latest Apranax clinical trials