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Fentora adverse events reported to FDA.

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Summary

FDA Adverse Reports: 208. View All

Fentora FDA safety alerts: 2007

Reported deaths: 41

Reported hospitalizations: 26

Fentora Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Fentora, 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 Fentora users, Learn more about unwanted side effects & find ways to reduce them. Browse Fentora Adverse Reports reported to FDA and participate in Fentora discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Fentora. 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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Fentora Adverse Effect Reports (FDA)

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6287481-6 | Abdominal Pain, Chest Pain, Faecaloma, Nausea
on Jul 15, 2009 Male patient from UNITED STATES , 57 years of age, weighting 150.6 lb, was diagnosed with cancer pain and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), chest pain (What is chest pain?), faecaloma, nausea (What is nausea?). Fentora dosage: See Image. During the same period patient was treated with ERLOTINIB (ERLOTINIB) (View Erlotinib (erlotinib) Review and Erlotinib (erlotinib) Label ), COMPAZINE (View Compazine Review and Compazine Label ), SENOKOT (SENNA ALEXANDRINA) (View Senokot (senna Alexandrina) Review and Senokot (senna Alexandrina) Label ), FLEET ENEMA (PARAFFIN, LIQUID) (View Fleet Enema (paraffin, Liquid) Review and Fleet Enema (paraffin, Liquid) Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ). Patient was hospitalized.

6285647-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Amylase Increased
Patient was taking Fentora (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood amylase increased on Jul 16, 2009 from UNITED STATES Additional patient health information: Female patient , 21 years of age, weighting 95.00 lb, was diagnosed with gastrointestinal pain and. Fentora dosage: 800 Mg, Bu. During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ).

6243954-3 | Alcohol Use, Cyanosis, Respiratory Depression, Unresponsive To Stimuli
Adverse event was reported on Jun 08, 2009 by a Male patient taking Fentora (View Usage) (Dosage: 800 Mcg (800 Mcg, 1 In 1 As Required) Bu) was diagnosed with breakthrough pain and. Location: UNITED STATES , 52 years of age, weighting 198.0 lb, After Fentora was administered, patient had the following side effects: alcohol use, cyanosis, respiratory depression, unresponsive to stimuli. During the same period patient was treated with OXYCODONE HYDROCHLORIDE (View Oxycodone Hydrochloride Review and Oxycodone Hydrochloride Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ). Patient was hospitalized.

6243953-1 | Application Site Reaction, Contraindication To Medical Treatment
on Jun 09, 2009 Male patient from UNITED STATES , 46 years of age, was diagnosed with migraine (What is migraine?) and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: application site reaction, contraindication to medical treatment. Fentora dosage: 400 Mcg (400 Mcg, 1 In 1 As Required), Bu 600 Mcg (600 Mcg, 1 In 1 As Required) Bu. During the same period patient was treated with AVINZA (View Avinza Review and Avinza Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), LAMOTRIGINE (View Lamotrigine Review and Lamotrigine Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), PHENERGAN (PROMETHAZINE) (View Phenergan (promethazine) Review and Phenergan (promethazine) Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), EXCEDRIN MIGRAINE (ACETYLSALICYLIC ACID, CAFFEINE, PARACETAMOL) (View Excedrin Migraine (acetylsalicylic Acid, Caffeine, Paracetamol) Review and Excedrin Migraine (acetylsalicylic Acid, Caffeine, Paracetamol) Label ).


6220246-X | Dyspnoea, Lung Disorder, Lung Infection, Malignant Neoplasm Progression
on May 29, 2009 Male patient from FRANCE , 67 years of age, was diagnosed with cancer pain and was treated with Fentora (View Usage). Patient had the following side effects: dyspnoea, lung disorder, lung infection, malignant neoplasm progression. Fentora dosage: 2400 Mcg (600 Mcg,4 In 1 D), Bu. During the same period patient was treated with FENTANYL (FENTANYL) (POULTICE OR PATCH) (View Fentanyl (fentanyl) (poultice Or Patch) Review and Fentanyl (fentanyl) (poultice Or Patch) Label ). Patient was hospitalized.

6215448-2 | Treatment Noncompliance, Withdrawal Syndrome
Patient was taking Fentora (View Usage). After Fentora was administered, patient had the following side effects: treatment noncompliance, withdrawal syndrome on May 26, 2009 from UNITED STATES Additional patient health information: Male patient , 58 years of age, weighting 183.0 lb, was diagnosed with pain (What is pain?) and. Fentora dosage: 200 Mcg (200 Mcg, 1 In 1 As Required), Bu. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), PERCOCET (View Percocet Review and Percocet Label ), OXYCODONE HYDROCHLORIDE (View Oxycodone Hydrochloride Review and Oxycodone Hydrochloride Label ).

6212466-5 | Dyspnoea, Lung Disorder, Lung Infection
Adverse event was reported on May 20, 2009 by a Male patient taking Fentora (View Usage) (Dosage: 2400 Mcg (600 Mcg, 4 In 1 D), Bu) was diagnosed with cancer pain and. Location: FRANCE , 67 years of age, Patient experienced the following unwanted or unexpected effects: dyspnoea, lung disorder, lung infection. During the same period patient was treated with FENTANYL (FENTANYL) (POULTICE OR PATCH) (View Fentanyl (fentanyl) (poultice Or Patch) Review and Fentanyl (fentanyl) (poultice Or Patch) Label ). Patient was hospitalized.

6197337-5 | Feeling Of Body Temperature Change, Inadequate Analgesia, Incorrect Dose Administered, Muscle Spasms, Pyrexia
on May 07, 2009 Male patient from UNITED STATES , 48 years of age, weighting 130.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). Patient had the following side effects: feeling of body temperature change, inadequate analgesia, incorrect dose administered, muscle spasms, pyrexia. Fentora dosage: 2800 Mcg (400 Mcg, 7 In 1 D), Bu, (800 Mcg) , Bu. During the same period patient was treated with SOMA (View Soma Review and Soma Label ), VICODIN (View Vicodin Review and Vicodin Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

6180320-3 | Tablet Issue, Therapeutic Response Unexpected
on May 04, 2009 Male patient from UNITED STATES , 47 years of age, weighting 270.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: tablet issue, therapeutic response unexpected. Fentora dosage: 400 Mcg. Every 6 Hrs..

6175341-0 | Diarrhoea, Feeling Of Body Temperature Change, Muscle Spasms, Nausea, Pyrexia
Patient was taking Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, feeling of body temperature change, muscle spasms, nausea (What is nausea?), pyrexia on Apr 15, 2009 from UNITED STATES Additional patient health information: Male patient , 48 years of age, weighting 130.0 lb, was diagnosed with pain (What is pain?) and. Fentora dosage: 2800 Mcg (400 Mcg, 7 In 1 D), Bu, 800 Mcg, Bu. During the same period patient was treated with SOMA (View Soma Review and Soma Label ), VICODIN (View Vicodin Review and Vicodin Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

6166589-X | Incorrect Dose Administered
Adverse event was reported on Apr 17, 2009 by a Female patient taking Fentora (View Usage) (Dosage: 800 Mcg, 2-3 Tablets Every 6-8 Hours, Bu) was diagnosed with neuralgia, muscle spasms and. Location: UNITED STATES , 48 years of age, Patient had the following side effects: incorrect dose administered. During the same period patient was treated with SOMA (350 Mg (350 Mg, 1 In 1 As Required), Oral) (View Soma Review and Soma Label ), DILAUDID (View Dilaudid Review and Dilaudid Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ).

6160488-5 | Treatment Noncompliance
on Apr 03, 2009 Male patient from UNITED STATES , 58 years of age, weighting 183.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: treatment noncompliance. Fentora dosage: 200 Mcg (200 Mcg, 1 In 1 As Required), Bu. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), PERCOCET (View Percocet Review and Percocet Label ), OXYIR (OXYCODONE HYDROCHLORIDE) (View Oxyir (oxycodone Hydrochloride) Review and Oxyir (oxycodone Hydrochloride) Label ).

6157779-0 | Refusal Of Treatment By Patient
on Apr 02, 2009 Male patient from UNITED STATES , 29 years of age, was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: refusal of treatment by patient. Fentora dosage: Bu.

6157778-9 | Cyanosis, Respiratory Depression, Vomiting Projectile
Patient was taking Fentora (View Usage). Patient had the following side effects: cyanosis, respiratory depression, vomiting projectile on Apr 02, 2009 from UNITED STATES Additional patient health information: Male patient , 21 years of age, . Fentora dosage: Bu.

6157771-6 | Accidental Exposure, Blood Pressure Systolic Increased, Drooling, Electrocardiogram Abnormal, Heart Rate Increased, Lethargy, Mental Status Changes, No Therapeutic Response
Adverse event was reported on Apr 02, 2009 by a Female patient taking Fentora (View Usage) (Dosage: (4 In 1 D), Bu) . Location: UNITED STATES , 60 years of age, After Fentora was administered, patient had the following side effects: accidental exposure, blood pressure systolic increased, drooling, electrocardiogram abnormal, heart rate increased, lethargy, mental status changes, no therapeutic response. During the same period patient was treated with LYRICA (View Lyrica Review and Lyrica Label ), MORPHINE (View Morphine Review and Morphine Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ATIVAN (View Ativan Review and Ativan Label ), TRILEPTAL (View Trileptal Review and Trileptal Label ), LASIX (View Lasix Review and Lasix Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

6155225-4 | Dental Caries, Tooth Disorder
on Apr 10, 2009 Male patient from UNITED STATES , 58 years of age, weighting 180.0 lb, was diagnosed with fibromyalgia and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: dental caries, tooth disorder (What is tooth disorder?). Fentora dosage: .

6152929-4 | Anxiety, Hyperventilation, Pain, Tremor
on Mar 30, 2009 Female patient from UNITED STATES , 45 years of age, was diagnosed with back pain (What is back pain?), scoliosis, spinal column stenosis and was treated with Fentora (View Usage). Patient had the following side effects: anxiety (What is anxiety?), hyperventilation, pain (What is pain?), tremor. Fentora dosage: 12000 Mcg (800 Mcg, 15 In 1 D), Bu. During the same period patient was treated with AVINZA (View Avinza Review and Avinza Label ), SKELAXIN (View Skelaxin Review and Skelaxin Label ). Patient was hospitalized and became disabled.

6138402-8 | Anxiety, Diarrhoea, Hyperventilation, Pain, Tremor
Patient was taking Fentora (View Usage). After Fentora was administered, patient had the following side effects: anxiety (What is anxiety?), diarrhoea, hyperventilation, pain (What is pain?), tremor on Mar 13, 2009 from UNITED STATES Additional patient health information: Female patient , 45 years of age, was diagnosed with back pain (What is back pain?), scoliosis, spinal column stenosis and. Fentora dosage: 12000 Mcg (800 Mcg, 15 In 1 D), Bu. During the same period patient was treated with AVINZA (View Avinza Review and Avinza Label ), SKELAXIN (View Skelaxin Review and Skelaxin Label ).

6137756-6 | Oral Pain
Adverse event was reported on Mar 12, 2009 by a Female patient taking Fentora (View Usage) (Dosage: Bu) was diagnosed with pain (What is pain?) and. Location: UNITED STATES , 42 years of age, Patient experienced the following unwanted or unexpected effects: oral pain.

6137151-X | Abdominal Pain, Anxiety, Arthralgia, Back Pain, Blood Blister, Chills, Cold Sweat, Confusional State, Constipation
on Mar 11, 2009 Female patient from UNITED STATES , 49 years of age, weighting 149.9 lb, was diagnosed with back pain (What is back pain?), fibromyalgia, neck pain and was treated with Fentora (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), anxiety (What is anxiety?), arthralgia, back pain (What is back pain?), blood blister, chills, cold sweat, confusional state, constipation (What is constipation?). Fentora dosage: Up To Four Tablets Qd Prn. During the same period patient was treated with FENTANYL CITRATE (FENTANYL CITRATE) (800 MICROGRAM, LOZENGE) (View Fentanyl Citrate (fentanyl Citrate) (800 Microgram, Lozenge) Review and Fentanyl Citrate (fentanyl Citrate) (800 Microgram, Lozenge) Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ).

6137110-7 | Arthralgia, Back Pain, Blood Blister, Constipation, Depression, Dry Mouth
on Mar 11, 2009 Female patient from UNITED STATES , 49 years of age, weighting 149.9 lb, was diagnosed with back pain (What is back pain?), fibromyalgia, neck pain and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: arthralgia, back pain (What is back pain?), blood blister, constipation (What is constipation?), depression (What is depression?), dry mouth. Fentora dosage: Up To Four Tablets Qd Prn (400 Mcg, 14 In 1 D), Bu. During the same period patient was treated with FENTANYL CITRATE (FENTANYL CITRATE) (800 MICROGRAM, LOZENGE) (View Fentanyl Citrate (fentanyl Citrate) (800 Microgram, Lozenge) Review and Fentanyl Citrate (fentanyl Citrate) (800 Microgram, Lozenge) Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ).

6130496-9 | Condition Aggravated, Dental Caries, Dry Mouth
Patient was taking Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, dental caries, dry mouth on Mar 09, 2009 from UNITED STATES Additional patient health information: Male patient , 53 years of age, weighting 222.0 lb, was diagnosed with back pain (What is back pain?) and. Fentora dosage: (200 Mcg, Qis As Needed), Bu. During the same period patient was treated with ATIVAN (View Ativan Review and Ativan Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ), TOFRANIL (View Tofranil Review and Tofranil Label ), PRIALT (View Prialt Review and Prialt Label ).

6130456-8 | Condition Aggravated, Dental Caries, Dry Mouth
Adverse event was reported on Mar 09, 2009 by a Male patient taking Fentora (View Usage) (Dosage: (200 Mcg, Qid As Needed), Bu) was diagnosed with back pain (What is back pain?) and. Location: UNITED STATES , 53 years of age, weighting 222.0 lb, Patient had the following side effects: condition aggravated, dental caries, dry mouth. During the same period patient was treated with ATIVAN (View Ativan Review and Ativan Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ), TOFRANIL (View Tofranil Review and Tofranil Label ), PRIALT (View Prialt Review and Prialt Label ).

6122004-3 | Condition Aggravated, Musculoskeletal Stiffness, Pain
on Mar 04, 2009 Male patient from UNITED STATES , 62 years of age, weighting 170.0 lb, was diagnosed with guillain-barre syndrome (What is guillain-barre syndrome?), pain (What is pain?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: condition aggravated, musculoskeletal stiffness, pain (What is pain?). Fentora dosage: 800 Ug Qid Prn Buccal. During the same period patient was treated with ACTIQ (View Actiq Review and Actiq Label ), NEURONTIN (View Neurontin Review and Neurontin Label ).

6115856-4 | Contraindication To Medical Treatment, No Therapeutic Response
on Feb 26, 2009 Male patient from UNITED STATES , weighting 260.0 lb, was diagnosed with migraine (What is migraine?) and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: contraindication to medical treatment, no therapeutic response. Fentora dosage: 800 Ug Bid Prn Buccal. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), IMITREX /01044801/ (View Imitrex /01044801/ Review and Imitrex /01044801/ Label ), PERCOCET (View Percocet Review and Percocet Label ).

6101081-X | Off Label Use
Patient was taking Fentora (View Usage). Patient had the following side effects: off label use on Feb 17, 2009 from UNITED STATES Additional patient health information: Female patient , 80 years of age, weighting 150.0 lb, was diagnosed with headache (What is headache?) and. Fentora dosage: 300 Ug Buccal. During the same period patient was treated with FENTANYL 25 (View Fentanyl-25 Review and Fentanyl-25 Label ), MORPHINE (View Morphine Review and Morphine Label ), TOPAMAX (View Topamax Review and Topamax Label ), SINEMET (View Sinemet Review and Sinemet Label ), EVISTA (View Evista Review and Evista Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ).

6094839-7 | Oral Discomfort, Oral Disorder
Adverse event was reported on Feb 13, 2009 by a Female patient taking Fentora (View Usage) (Dosage: 200 Ug Buccal) was diagnosed with ocular neoplasm and. Location: UNITED STATES , 49 years of age, weighting 99.00 lb, After Fentora was administered, patient had the following side effects: oral discomfort, oral disorder. During the same period patient was treated with BUTALBITAL/ASA/CODEINE (View Butalbital/asa/codeine Review and Butalbital/asa/codeine Label ), ORGANIDIN NR (View Organidin Nr Review and Organidin Nr Label ), BECONASE AQ (View Beconase Aq Review and Beconase Aq Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), VIGAMOX (View Vigamox Review and Vigamox Label ), GENTEAL (View Genteal Review and Genteal Label ), NASONEX (View Nasonex Review and Nasonex Label ), LOMOTIL (View Lomotil Review and Lomotil Label ).

6083558-9 | Therapeutic Response Decreased
on Feb 04, 2009 Male patient from UNITED STATES , 64 years of age, weighting 168.0 lb, was diagnosed with bone pain and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: therapeutic response decreased. Fentora dosage: 600 Ug Buccal. During the same period patient was treated with OPANA (View Opana Review and Opana Label ), VALIUM (View Valium Review and Valium Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), DHEA SR (View Dhea Sr Review and Dhea Sr Label ), AMBIEN (View Ambien Review and Ambien Label ).

6067769-4 | Product Quality Issue, Treatment Noncompliance
on Jan 21, 2009 Female patient from UNITED STATES , 49 years of age, weighting 158.0 lb, was diagnosed with extrinsic vascular compression, neoplasm, nerve compression and was treated with Fentora (View Usage). Patient had the following side effects: product quality issue, treatment noncompliance. Fentora dosage: 800 Ug Qid Buccal. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), PHENERGAN HCL (View Phenergan Hcl Review and Phenergan Hcl Label ).

6067768-2 | Tooth Disorder
Patient was taking Fentora (View Usage). After Fentora was administered, patient had the following side effects: tooth disorder (What is tooth disorder?) on Jan 23, 2009 from UNITED STATES Additional patient health information: Male patient , 43 years of age, was diagnosed with pain (What is pain?) and. Fentora dosage: 400 Ug Bid Buccal. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ).

6063985-6 | Accidental Exposure, Heart Rate Increased, Respiratory Rate Increased, Somnolence
Adverse event was reported on Jan 16, 2009 by a Female patient taking Fentora (View Usage) (Dosage: Once Buccal) . Location: UNITED STATES , child 1 years of age, Patient experienced the following unwanted or unexpected effects: accidental exposure, heart rate increased, respiratory rate increased, somnolence. Patient was hospitalized.

6063922-4 | Accidental Exposure, Lethargy, Vomiting
on Jan 16, 2009 Male patient from UNITED STATES , 71 years of age, was treated with Fentora (View Usage). Patient had the following side effects: accidental exposure, lethargy, vomiting. Fentora dosage: One Buccal.

6063568-8 | Gingivitis
on Jan 20, 2009 Male patient from UNITED STATES , 67 years of age, weighting 136.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: gingivitis. Fentora dosage: 600 Ug Q 3-6 Hrs Prn Buccal. During the same period patient was treated with CODEINE (View Codeine Review and Codeine Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), KADIAN (View Kadian Review and Kadian Label ).

6063566-4 |
Patient was taking Fentora (View Usage). on Jan 22, 2009 from UNITED STATES Additional patient health information: Female patient , 51 years of age, was diagnosed with cancer pain and. Fentora dosage: 800 Ug Tid Buccal. During the same period patient was treated with FENTANYL 75 (View Fentanyl-75 Review and Fentanyl-75 Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ).

6063565-2 | Accidental Exposure
Adverse event was reported on Jan 16, 2009 by a Female patient taking Fentora (View Usage) (Dosage: Once Buccal) . Location: UNITED STATES , child 6 years of age, Patient had the following side effects: accidental exposure.

6039505-9 | Dyspnoea, Somnolence
on Jan 06, 2009 Male patient from UNITED STATES , 24 years of age, was diagnosed with headache (What is headache?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: dyspnoea, somnolence. Fentora dosage: 2 Or 3 Occasions.

6026609-X | Abdominal Pain, Chest Pain, Faecaloma, Nausea
on Dec 16, 2008 Male patient from UNITED STATES , 57 years of age, was diagnosed with cancer pain, non-small cell lung cancer and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), chest pain (What is chest pain?), faecaloma, nausea (What is nausea?). Fentora dosage: 400 Ug 400ug Q6hr As Needed Buccal. During the same period patient was treated with ERLOTINIB (150 Mg Qd Oral) (View Erlotinib Review and Erlotinib Label ), COMPAZINE /00013302/ (View Compazine /00013302/ Review and Compazine /00013302/ Label ), SENOKOT /00142201/ (View Senokot /00142201/ Review and Senokot /00142201/ Label ), FLEET ENEMA /00103901/ (View Fleet Enema /00103901/ Review and Fleet Enema /00103901/ Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ). Patient was hospitalized.

6026148-6 | Completed Suicide
Patient was taking Fentora (View Usage). Patient had the following side effects: completed suicide on Dec 22, 2008 from UNITED STATES Additional patient health information: Male patient , 28 years of age, . Fentora dosage: Buccal. During the same period patient was treated with ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ).

6026067-5 | Accidental Overdose, Somnolence, Suicidal Behaviour, Suicide Attempt
Adverse event was reported on Dec 15, 2008 by a Female patient taking Fentora (View Usage) (Dosage: 400 Ug Buccal) was diagnosed with headache (What is headache?) and. Location: UNITED STATES , 34 years of age, weighting 169.0 lb, After Fentora was administered, patient had the following side effects: accidental overdose, somnolence, suicidal behaviour, suicide attempt. During the same period patient was treated with LUNESTA (View Lunesta Review and Lunesta Label ), VALIUM (View Valium Review and Valium Label ), TRAZODONE HCL (View Trazodone Hcl Review and Trazodone Hcl Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), AMBIEN (View Ambien Review and Ambien Label ).

6018757-5 | Fluid Retention, Ovarian Mass
on Dec 12, 2008 Female patient from UNITED STATES , 48 years of age, weighting 130.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: fluid retention, ovarian mass. Fentora dosage: 800 Ug 12 Tablets Daily Prn Buccal. During the same period patient was treated with ACTIQ (View Actiq Review and Actiq Label ), KLONOPIN (View Klonopin Review and Klonopin Label ), SOMA (View Soma Review and Soma Label ), AMBIEN (View Ambien Review and Ambien Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), BUMETANIDE (View Bumetanide Review and Bumetanide Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), VALTREX (View Valtrex Review and Valtrex Label ).

6010893-2 | Pulse Absent, Unresponsive To Stimuli
on Dec 09, 2008 Male patient from UNITED STATES , weighting 185.0 lb, was treated with Fentora (View Usage). Patient had the following side effects: pulse absent, unresponsive to stimuli. Fentora dosage: Buccal. During the same period patient was treated with OXYCODONE (View Oxycodone Review and Oxycodone Label ).

6009931-2 | Pulse Absent, Unresponsive To Stimuli
Patient was taking Fentora (View Usage). After Fentora was administered, patient had the following side effects: pulse absent, unresponsive to stimuli on Dec 09, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 185.0 lb, . Fentora dosage: Buccal. During the same period patient was treated with OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

5998018-0 | Product Quality Issue
Adverse event was reported on Dec 01, 2008 by a Male patient taking Fentora (View Usage) (Dosage: 400 Ug Qid Buccal) was diagnosed with complex regional pain syndrome (What is complex regional pain syndrome?) and. Location: UNITED STATES , 47 years of age, weighting 245.0 lb, Patient experienced the following unwanted or unexpected effects: product quality issue. During the same period patient was treated with NEURONTIN (View Neurontin Review and Neurontin Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), TOPAMAX (View Topamax Review and Topamax Label ), CELEBREX (View Celebrex Review and Celebrex Label ), TIZANIDINE HCL (View Tizanidine Hcl Review and Tizanidine Hcl Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), TRAZODONE (View Trazodone Review and Trazodone Label ), METHYLIN (View Methylin Review and Methylin Label ).

5991113-1 | Dental Caries, Sensitivity Of Teeth, Toothache
on Aug 26, 2008 Female patient from UNITED STATES , 35 years of age, weighting 218.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Fentora (View Usage). Patient had the following side effects: dental caries, sensitivity of teeth, toothache. Fentora dosage: 300 Ug Qid Prn Buccal. During the same period patient was treated with KADIAN (View Kadian Review and Kadian Label ), REMERON (View Remeron Review and Remeron Label ), LASIX (View Lasix Review and Lasix Label ), NEXIUM (View Nexium Review and Nexium Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), PRILOSEC (View Prilosec Review and Prilosec Label ).

5982146-X | Fatigue, Flushing, Tachycardia, Tremor, Vision Blurred
on Nov 24, 2008 Male patient from UNITED STATES , 60 years of age, weighting 220.0 lb, was diagnosed with pain (What is pain?) and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: fatigue, flushing, tachycardia, tremor, vision blurred. Fentora dosage: 400 Ug Qid Buccal. During the same period patient was treated with ACTIQ (Ug Tid Prn Buccal) (View Actiq Review and Actiq Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), AMRIX (View Amrix Review and Amrix Label ), TOPAMAX (View Topamax Review and Topamax Label ), BENICAR (View Benicar Review and Benicar Label ).

5974275-1 | Accidental Overdose, Somnolence, Suicidal Ideation
Patient was taking Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: accidental overdose, somnolence, suicidal ideation on Nov 21, 2008 from UNITED STATES Additional patient health information: Female patient , 34 years of age, weighting 169.0 lb, was diagnosed with headache (What is headache?) and. Fentora dosage: 400 Ug Unk Buccal.

5974272-6 | Abdominal Pain, Headache, Nausea, Product Quality Issue
Adverse event was reported on Nov 18, 2008 by a Female patient taking Fentora (View Usage) (Dosage: 200 Ug Every 6-8 Hour Prn Buccal) was diagnosed with hernia (What is hernia?) and. Location: UNITED STATES , 45 years of age, weighting 287.0 lb, Patient had the following side effects: abdominal pain (What is abdominal pain?), headache (What is headache?), nausea (What is nausea?), product quality issue. During the same period patient was treated with DOXYCYLINE (View Doxycyline Review and Doxycyline Label ), PHENERGAN HCL (View Phenergan Hcl Review and Phenergan Hcl Label ), PROTONIX (View Protonix Review and Protonix Label ), BUMEX (View Bumex Review and Bumex Label ).

5974270-2 | Abdominal Pain, Chest Pain, Condition Aggravated, Faecaloma, Nausea
on Nov 13, 2008 Male patient from UNITED STATES , 57 years of age, was diagnosed with cancer pain and was treated with Fentora (View Usage). After Fentora was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), chest pain (What is chest pain?), condition aggravated, faecaloma, nausea (What is nausea?). Fentora dosage: 400 Ug 400ug Q6hr As Needed Oral. Patient was hospitalized.

5960966-5 | Application Site Irritation
on Nov 07, 2008 Female patient from UNITED STATES , 53 years of age, weighting 145.0 lb, was diagnosed with fibromyalgia, guillain-barre syndrome (What is guillain-barre syndrome?) and was treated with Fentora (View Usage). Patient experienced the following unwanted or unexpected effects: application site irritation. Fentora dosage: 200 Ug Prn Buccal. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), PEPCID (View Pepcid Review and Pepcid Label ), ESTRACE (View Estrace Review and Estrace Label ).

5948730-4 | Abdominal Pain Upper, Product Quality Issue
Patient was taking Fentora (View Usage). Patient had the following side effects: abdominal pain upper, product quality issue on Oct 30, 2008 from UNITED STATES Additional patient health information: Male patient , 45 years of age, weighting 180.0 lb, was diagnosed with back pain (What is back pain?) and. Fentora dosage: 200 Ug Two To Four Tablets/day Buccal. During the same period patient was treated with NORCO (View Norco Review and Norco Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), DEPAKOTE (View Depakote Review and Depakote Label ).

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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 Fentora 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 Fentora quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fentora 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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Fentora Reactions
Abdominal PainWhat is Abdominal pain?
Accidental Exposure
Accidental Overdose
AnxietyWhat is Anxiety?
Application Site Irritation
Application Site Ulcer
Condition Aggravated
ConstipationWhat is Constipation?
Cyanosis
Death
Dental Caries
DepressionWhat is Depression?
DizzinessWhat is Dizziness?
Dysgeusia
Dyspnoea
Gingival Pain
Inadequate Analgesia
Incorrect Dose Administered
Loss Of Consciousness
Mouth Ulceration
NauseaWhat is Nausea?
Overdose
PainWhat is Pain?
Product Quality Issue
Respiratory Depression
Somnolence
Stomatitis
Tremor
Unresponsive To Stimuli
Vomiting
Fentora 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 Fentora 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!