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GABRIEL ANDRE 4 RUE TABARLY F-38500 VOIRON; THIS AFTERNOON MY WIFE UNDER MORPHINE ...Keep Reading

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Indicate Your Profenid Side Effects
Profenid (3)
Stomach Pains (2)
Difficult Breathing (1)
I Have Take 18 Bills Of Biprofenid (1)
Sleep (1)
Slight Bleeding After Every Urine Discharge (1)
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Common Profenid Side Effects

top 5 Profenid|Profenid|Stomach pa|Difficult |I have tak|Sleep|Slight ble adverse effects>>See All Profenid Side Effects

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Profenid adverse events reported to FDA.

Have You Experienced unusual Profenid symptoms? PatientsVille.com collects and analyzes Profenid side effect and adverse reports submitted by Profenid users, such as severe stomach pain |, GI bleeding.......... |.

Summary

FDA Adverse Reports: 17. View All

Profenid FDA safety alerts: No

Reported hospitalizations: 15

More About Profenid

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Most Reported
1Profenid
2Stomach Pains
3Slight Bleeding After Every Urine Discharge
4Difficult Breathing
5I Have Take 18 Bills Of Biprofenid
6Sleep
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severe stomach pain

, GI bleeding..........

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Often additional risks of using a medication, such as Profenid, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Profenid users, Learn more about unwanted side effects & find ways to reduce them. Browse Profenid Adverse Reports reported to FDA and participate in Profenid discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Profenid. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Profenid Adverse Effect Reports (FDA)

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6696575-2 | Anaemia, Gastric Ulcer, Injection Site Haematoma, International Normalised Ratio Increased, Melaena
on Apr 22, 2010 Male patient from FRANCE , 80 years of age, was diagnosed with spinal compression fracture and was treated with Profenid (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, gastric ulcer, injection site haematoma, international normalised ratio increased, melaena. Profenid dosage: Dose:50 Milligram(s)/millilitre. During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), PREVISCAN (View Previscan Review and Previscan Label ), COVERSYL /FRA/ (View Coversyl /fra/ Review and Coversyl /fra/ Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), ADANCOR (View Adancor Review and Adancor Label ), DISCOTRINE (View Discotrine Review and Discotrine Label ). Patient was hospitalized and became disabled.

6689874-1 | Anaemia, Gastric Ulcer, Injection Site Haematoma, International Normalised Ratio Increased, Melaena
Patient was taking Profenid (View Usage). Patient had the following side effects: anaemia, gastric ulcer, injection site haematoma, international normalised ratio increased, melaena on Apr 13, 2010 from FRANCE Additional patient health information: Male patient , 80 years of age, was diagnosed with spinal compression fracture and. Profenid dosage: Dose:50 Milligram(s)/millilitre. During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), PREVISCAN (View Previscan Review and Previscan Label ), COVERSYL /FRA/ (View Coversyl /fra/ Review and Coversyl /fra/ Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), ADANCOR (View Adancor Review and Adancor Label ), DISCOTRINE (View Discotrine Review and Discotrine Label ). Patient was hospitalized and became disabled.

6131897-5 | Chills, Feeling Hot, Headache, Tremor
Adverse event was reported on Mar 20, 2009 by a Female patient taking Profenid (View Usage) (Dosage: ) . Location: FRANCE , 48 years of age, After Profenid was administered, patient had the following side effects: chills, feeling hot, headache (What is headache?), tremor. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), CONTRAST MEDIA (View Contrast Media Review and Contrast Media Label ). Patient was hospitalized.

6115428-1 | Chills, Feeling Hot, Headache, Tremor
on Mar 04, 2009 Female patient from FRANCE , 48 years of age, was treated with Profenid (View Usage). Patient experienced the following unwanted or unexpected effects: chills, feeling hot, headache (What is headache?), tremor. Profenid dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), CONTRAST MEDIA (View Contrast Media Review and Contrast Media Label ). Patient was hospitalized.


6048651-5 | Hyperkalaemia, Renal Failure Chronic
on Jan 15, 2009 Female patient from , 73 years of age, was diagnosed with prophylaxis and was treated with Profenid (View Usage). Patient had the following side effects: hyperkalaemia, renal failure chronic. Profenid dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ). Patient was hospitalized.

5633082-X | Leukopenia, Neutropenia
Patient was taking Profenid (View Usage). After Profenid was administered, patient had the following side effects: leukopenia, neutropenia on Feb 12, 2008 from Additional patient health information: Female patient , 79 years of age, was diagnosed with prophylaxis, pancreatitis and. Profenid dosage: . During the same period patient was treated with ULTRACET (View Ultracet Review and Ultracet Label ), LOVENOX (View Lovenox Review and Lovenox Label ), NEXIUM (View Nexium Review and Nexium Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), DAFALGAN /00020001/ (View Dafalgan /00020001/ Review and Dafalgan /00020001/ Label ), CLAMOXYL /00249601/ (View Clamoxyl /00249601/ Review and Clamoxyl /00249601/ Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ). Patient was hospitalized.

5601531-9 | Leukopenia, Neutropenia
Adverse event was reported on Jan 18, 2008 by a Female patient taking Profenid (View Usage) (Dosage: ) was diagnosed with prophylaxis, pancreatitis and. Location: , 79 years of age, Patient experienced the following unwanted or unexpected effects: leukopenia, neutropenia. During the same period patient was treated with ULTRACET (View Ultracet Review and Ultracet Label ), LOVENOX (View Lovenox Review and Lovenox Label ), INEXIUM (View Inexium Review and Inexium Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), DAFALGAN /00020001/ (View Dafalgan /00020001/ Review and Dafalgan /00020001/ Label ), CLAMOXYL /00249601/ (View Clamoxyl /00249601/ Review and Clamoxyl /00249601/ Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), CEFACIDAL (View Cefacidal Review and Cefacidal Label ). Patient was hospitalized.

5598288-7 | Gastric Ulcer, Gastrointestinal Haemorrhage
on Jan 11, 2008 Female patient from , 80 years of age, was diagnosed with pain (What is pain?) and was treated with Profenid (View Usage). Patient had the following side effects: gastric ulcer, gastrointestinal haemorrhage. Profenid dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), DI ANTALVIC /00220901/ (View Di-antalvic /00220901/ Review and Di-antalvic /00220901/ Label ), ORBENINE (View Orbenine Review and Orbenine Label ), VENOFER (View Venofer Review and Venofer Label ), COAPROVEL (View Coaprovel Review and Coaprovel Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ), ALPRESS (View Alpress Review and Alpress Label ). Patient was hospitalized.

5581596-3 | Leukopenia, Neutropenia
on Dec 26, 2007 Female patient from , 79 years of age, was diagnosed with prophylaxis, pancreatitis and was treated with Profenid (View Usage). After Profenid was administered, patient had the following side effects: leukopenia, neutropenia. Profenid dosage: . During the same period patient was treated with ACETAMINOPHEN AND TRAMADOL HCL (View Acetaminophen And Tramadol Hcl Review and Acetaminophen And Tramadol Hcl Label ), LOVENOX (View Lovenox Review and Lovenox Label ), INEXIUM (View Inexium Review and Inexium Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), DAFALGAN /00020001/ (View Dafalgan /00020001/ Review and Dafalgan /00020001/ Label ), CLAMOXYL /00249601/ (View Clamoxyl /00249601/ Review and Clamoxyl /00249601/ Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), CEFACIDAL (View Cefacidal Review and Cefacidal Label ). Patient was hospitalized.

5464458-1 | Renal Failure Acute, Renal Tubular Necrosis
Patient was taking Profenid (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute, renal tubular necrosis on Sep 12, 2007 from Additional patient health information: Male patient , 55 years of age, weighting 121.3 lb, . Profenid dosage: . During the same period patient was treated with LASILIX /00032601/ (View Lasilix /00032601/ Review and Lasilix /00032601/ Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ). Patient was hospitalized.

5416607-9 | Dermatitis Bullous, Hypotension, Rash Erythematous, Stevens-johnson Syndrome
Adverse event was reported on Aug 09, 2007 by a Male patient taking Profenid (View Usage) (Dosage: ) was diagnosed with thrombosis prophylaxis and. Location: , 56 years of age, Patient had the following side effects: dermatitis bullous, hypotension, rash erythematous, stevens-johnson syndrome. During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), MYOLASTAN (View Myolastan Review and Myolastan Label ), PERFALGAN (Dose Quantity: 40; Daily Dose Unit: Milligram Per Millilitre) (View Perfalgan Review and Perfalgan Label ), DEBRIDAT /00465201/ (Dose Quantity: 40; Daily Dose Unit: Milligram Per Millilitre) (View Debridat /00465201/ Review and Debridat /00465201/ Label ), NIMBEX (View Nimbex Review and Nimbex Label ), ULTIVA (View Ultiva Review and Ultiva Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ).

5387424-3 | Dermatitis Bullous, Hypotension, Rash Erythematous, Stevens-johnson Syndrome
on Jul 06, 2007 Male patient from , 56 years of age, was diagnosed with anaesthesia and was treated with Profenid (View Usage). After Profenid was administered, patient had the following side effects: dermatitis bullous, hypotension, rash erythematous, stevens-johnson syndrome. Profenid dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), MYOLASTAN (View Myolastan Review and Myolastan Label ), PERFALGAN (Dose Quantity: 40; Daily Dose Unit: Milligram Per Millilitre) (View Perfalgan Review and Perfalgan Label ), DEBRIDAT /00465201/ (Dose Quantity: 40; Daily Dose Unit: Milligram Per Millilitre) (View Debridat /00465201/ Review and Debridat /00465201/ Label ), NIMBEX (View Nimbex Review and Nimbex Label ), ULTIVA (View Ultiva Review and Ultiva Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ).

5376034-X | Renal Failure Acute, Renal Tubular Necrosis
on Jun 25, 2007 Male patient from , 55 years of age, weighting 121.3 lb, was treated with Profenid (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute, renal tubular necrosis. Profenid dosage: . During the same period patient was treated with LASILIX /00032601/ (View Lasilix /00032601/ Review and Lasilix /00032601/ Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ). Patient was hospitalized.

4847036-4 | Renal Failure Acute
Patient was taking Profenid (View Usage). Patient had the following side effects: renal failure acute on Nov 15, 2005 from JAPAN Additional patient health information: Male patient , 30 years of age, was diagnosed with back pain (What is back pain?) and. Profenid dosage: . During the same period patient was treated with ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ), SPASFON (View Spasfon Review and Spasfon Label ). Patient was hospitalized.

4833306-2 | Renal Failure Acute
Adverse event was reported on Nov 15, 2005 by a Male patient taking Profenid (View Usage) (Dosage: ) was diagnosed with back pain (What is back pain?) and. Location: JAPAN , 30 years of age, After Profenid was administered, patient had the following side effects: renal failure acute. During the same period patient was treated with ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ), SPASFON (View Spasfon Review and Spasfon Label ). Patient was hospitalized.

4810943-2 | Gastric Ulcer, Gastrointestinal Haemorrhage
on Oct 20, 2005 Male patient from JAPAN , 65 years of age, was diagnosed with diabetes mellitus, essential hypertension and was treated with Profenid (View Usage). Patient experienced the following unwanted or unexpected effects: gastric ulcer, gastrointestinal haemorrhage. Profenid dosage: . During the same period patient was treated with OMEPRAZOLE (Gastro-resistant Capsules) (View Omeprazole Review and Omeprazole Label ), CLOPIDOGREL BISULFATE (Film-coated Tablets) (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), METFORMIN EMBONATE (View Metformin Embonate Review and Metformin Embonate Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), REPAGLINIDE (View Repaglinide Review and Repaglinide Label ). Patient was hospitalized.

4774894-4 | Acute Respiratory Distress Syndrome, Anuria, Back Pain, Calculus Ureteric, Culture Urine Positive, Escherichia Infection, Escherichia Sepsis, Pyelonephritis, Renal Colic
on Sep 13, 2005 Female patient from , 76 years of age, weighting 242.5 lb, was diagnosed with abdominal pain (What is abdominal pain?), diabetes mellitus non-insulin-dependent and was treated with Profenid (View Usage). Patient had the following side effects: acute respiratory distress syndrome, anuria, back pain (What is back pain?), calculus ureteric, culture urine positive, escherichia infection, escherichia sepsis, pyelonephritis, renal colic. Profenid dosage: . During the same period patient was treated with AMAREL (View Amarel Review and Amarel Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), SPASFON (View Spasfon Review and Spasfon Label ). Patient was hospitalized.


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Profenid Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

omaziz   Kuwait

8:50am on Wednesday, December 21st, 2011

I'm pregnant in 39 weeks
and i took 2 tablets of profenid, after 4 hours i took 2 more
it is ok ? ... read more »

melvin   kingston

1:37pm on Monday, February 22nd, 2010

I am 50 years old and suffering from sciatica pains is it ok for me to take profenid 150

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Profenid risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Profenid quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Profenid use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Profenid Reactions
Acute Respiratory Distress Syndrome
Anaemia
Anuria
Back PainWhat is Back pain?
Calculus Ureteric
Chills
Culture Urine Positive
Dermatitis Bullous
Escherichia Infection
Escherichia Sepsis
Feeling Hot
Gastric Ulcer
Gastrointestinal Haemorrhage
HeadacheWhat is Headache?
Hyperkalaemia
Hypotension
Injection Site Haematoma
International Normalised Ratio Increased
Leukopenia
Melaena
Neutropenia
Pyelonephritis
Rash Erythematous
Renal Colic
Renal Failure Acute
Renal Failure Chronic
Renal Tubular Necrosis
Stevens-johnson Syndrome
Tremor
Profenid Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Profenid adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!