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Morphine Side Effects Report #5654425-7
Consumer or non-health professional from UNITED STATES reported MORPHINE SULPHATE problem on Feb 26, 2008. Male patient, 27 years of age, weighting 380.0 lb, was diagnosed with back pain, headache and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, headache, hypertensive heart disease, neck pain, peripheral coldness, unresponsive to stimuli, . MORPHINE SULPHATE dosage: unknown. During the same period patient was treated with MORPHINE SULPHATE, MORPHINE SULPHATE, MORPHINE SULPHATE, NORCO, XANAX, KLONOPIN. Patient died on 11/24/2007.

Fentanyl Side Effects Report #5671053-8
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 27, 2008. Female patient, 33 years of age, was diagnosed with back pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, hyperhidrosis, influenza like illness, loss of consciousness, memory impairment, overdose, pyrexia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with BACLOFEN, CYMBALTA. Patient recovered.

Amitriptyline Side Effects Report #5613194-7
Health Professional from PORTUGAL reported AMITRIPTYLINE HYDROCHLORIDE problem on Jan 10, 2008. Female patient, 44 years of age, was treated with AMITRIPTYLINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, visceral congestion, vomiting, . AMITRIPTYLINE HYDROCHLORIDE dosage: unknown. Patient died.

Claritin Side Effects Report #5566505-5
CLARITIN problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 03, 2007. Male patient was treated with CLARITIN. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, overdose, somnolence, . CLARITIN dosage: unknown. Patient recovered.


Commit Side Effects Report #5516353-7
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Feb 06, 2007. Female patient, 58 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, nausea, oral discomfort, productive cough, . COMMIT dosage: unknown. During the same period patient was treated with NICORETTE. Patient recovered.

Amitriptyline Side Effects Report #5491344-3
AMITRIPTYLINE problem was reported by a Health Professional from PORTUGAL on Oct 05, 2007. Female patient, 44 years of age, was treated with AMITRIPTYLINE. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, oesophageal disorder, tongue disorder, visceral congestion, vomiting, . AMITRIPTYLINE dosage: unknown. During the same period patient was treated with DIAZEPAM. Patient died.

Daktarin Side Effects Report #5383892-1
Consumer or non-health professional from BRAZIL reported DAKTARIN GEL problem on July 02, 2007. Male patient, weighting 8.82 lb, was diagnosed with oral candidiasis and was treated with DAKTARIN GEL. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, . DAKTARIN GEL dosage: unknown. During the same period patient was treated with DAKTARIN GEL. Patient recovered.

Target Side Effects Report #5388145-3
TARGET ORIGINAL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 19, 2006. Male patient, 33 years of age, was treated with TARGET ORIGINAL. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, . TARGET ORIGINAL dosage: unknown. Patient recovered.

Ultravist Side Effects Report #5399470-4
Health Professional from UNITED STATES reported ULTRAVIST problem on July 23, 2007. Male patient, 60 years of age, weighting 249.1 lb, was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, micturition urgency, speech disorder, unevaluable event, . ULTRAVIST dosage: 100 ML, 1 DOSE. During the same period patient was treated with TRIAMTERENE, QUINAPRIL, HYDROCHLOROTHIAZIDE, CONTRAST MEDIA. Patient was hospitalized. Patient died on 11/06/2006.


Daktarin Side Effects Report #5383892-1
DAKTARIN GEL problem was reported by a Consumer or non-health professional from BRAZIL on July 02, 2007. Male patient, weighting 8.82 lb, was diagnosed with oral candidiasis and was treated with DAKTARIN GEL. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, . DAKTARIN GEL dosage: unknown. During the same period patient was treated with DAKTARIN GEL. Patient recovered.

Target Side Effects Report #5388145-3
Consumer or non-health professional from UNITED STATES reported TARGET ORIGINAL problem on Dec 19, 2006. Male patient, 33 years of age, was treated with TARGET ORIGINAL. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, . TARGET ORIGINAL dosage: unknown. Patient recovered.

Ultravist Side Effects Report #5399470-4
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on July 23, 2007. Male patient, 60 years of age, weighting 249.1 lb, was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, micturition urgency, speech disorder, unevaluable event, . ULTRAVIST dosage: 100 ML, 1 DOSE. During the same period patient was treated with TRIAMTERENE, QUINAPRIL, HYDROCHLOROTHIAZIDE, CONTRAST MEDIA. Patient was hospitalized. Patient died on 11/06/2006.

Avelox Side Effects Report #5740306-7
Consumer or non-health professional from UNITED STATES reported AVELOX problem on May 08, 2008. Female patient, 84 years of age, was diagnosed with lower respiratory tract infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, loss of consciousness, oedema peripheral, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with SOTALOL, LASIX, COUMADIN, DIGOXIN. Patient recovered.

Hydrogen Side Effects Report #5323929-9
HYDROGEN PEROXIDE SOLUTION problem was reported by a Consumer or non-health professional from UNITED STATES on May 09, 2007. Female patient was treated with HYDROGEN PEROXIDE SOLUTION. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, retching, . HYDROGEN PEROXIDE SOLUTION dosage: unknown. Patient recovered.


Humulin Side Effects Report #5261105-9
Consumer or non-health professional from UNITED STATES reported HUMULIN N problem on Mar 02, 2007. Female patient, 75 years of age, was diagnosed with diabetes mellitus and was treated with HUMULIN N. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, gallbladder operation, gastric disorder, stomach discomfort, . HUMULIN N dosage: unknown. During the same period patient was treated with ZOCOR, COZAAR, FOLIC ACID, ASPIRIN, HUMULIN R. Patient was hospitalized. Patient recovered.

Ultravist Side Effects Report #5264228-3
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on Feb 07, 2007. Male patient, 60 years of age, weighting 249.1 lb, was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, micturition urgency, speech disorder, unevaluable event, . ULTRAVIST dosage: 100 ML, 1 DOSE. During the same period patient was treated with TRIAMTERENE, QUINAPRIL, HYDROCHLOROTHIAZIDE, CONTRAST MEDIA. Patient was hospitalized. Patient died on 11/06/2006.

Fentanyl Side Effects Report #5648123-3
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 22, 2008. Female patient, weighting 168.0 lb, was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, overdose, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5661776-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, weighting 168.0 lb, was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, overdose, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient was hospitalized. Patient recovered.

Amoxicillin Side Effects Report #5679055-2
Health Professional from UNITED STATES reported AMOXICILLIN problem on Mar 24, 2008. Female patient was treated with AMOXICILLIN. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, hypotonia, incorrect dose administered, vomiting, . AMOXICILLIN dosage: unknown. Patient recovered.


Clonidine Side Effects Report #5479282-3
CLONIDINE problem was reported by a Physician from UNITED STATES on Sept 18, 2007. Female patient, child 6 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CLONIDINE. After drug was administered, patient experienced the following problems/side effects: depressed level of consciousness, foaming at mouth, overdose, pulse absent, . CLONIDINE dosage: 0.05 MG; 3 TIMES A DAY; ORAL; 0.2 MG AT BEDTIME; ORAL. During the same period patient was treated with OPOIDS, VALPROIC, CHLORPHENIRAMINE, DEXTROMETHORPHAN HYDROBROMIDE. Patient died on 12/13/2006.

Maalox Side Effects Report #5773057-3
Consumer or non-health professional from UNITED STATES reported MAALOX MS TOTAL STOMACH RELIEF problem on June 03, 2008. Male patient, 75 years of age, weighting 239.9 lb, was diagnosed with dyspepsia, flatulence and was treated with MAALOX MS TOTAL STOMACH RELIEF. After drug was administered, patient experienced the following problems/side effects: constipation, foaming at mouth, myocardial infarction, . MAALOX MS TOTAL STOMACH RELIEF dosage: unknown. During the same period patient was treated with MAALOX MS TOTAL STOMACH RELIEF. Patient was hospitalized. Patient recovered.

Maalox Side Effects Report #5796599-3
MAALOX TOTAL STOMACH RELIEF problem was reported by a Consumer or non-health professional from UNITED STATES on June 20, 2008. Male patient, 75 years of age, weighting 239.9 lb, was diagnosed with dyspepsia, flatulence and was treated with MAALOX TOTAL STOMACH RELIEF. After drug was administered, patient experienced the following problems/side effects: constipation, foaming at mouth, myocardial infarction, . MAALOX TOTAL STOMACH RELIEF dosage: unknown. During the same period patient was treated with MAALOX TOTAL STOMACH RELIEF. Patient was hospitalized. Patient recovered.

Lamictal Side Effects Report #5746442-3
Consumer or non-health professional from NORWAY reported LAMICTAL problem on May 19, 2008. Female patient, 16 years of age, was diagnosed with epilepsy and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: epilepsy, foaming at mouth, pulmonary haemorrhage, pulmonary oedema, . LAMICTAL dosage: unknown. Patient died on 11/09/2002.

Implanon Side Effects Report #5694083-9
IMPLANON problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2008. Female patient, 19 years of age, weighting 179.9 lb, was diagnosed with contraception and was treated with IMPLANON. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, mood swings, . IMPLANON dosage: unknown. Patient recovered.

Singulair Side Effects Report #5720521-9
Consumer or non-health professional from UNITED STATES reported SINGULAIR problem on Jan 17, 2008. Female patient, child 4 years of age, was diagnosed with ear infection and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, . SINGULAIR dosage: unknown. During the same period patient was treated with PULMICORT, ROBITUSSIN, XOPENEX, ZITHROMAX. Patient recovered.

Nexium Side Effects Report #5721834-7
NEXIUM problem was reported by a Consumer or non-health professional from UNITED STATES on June 14, 2007. Female patient, 34 years of age, weighting 215.0 lb, was diagnosed with pharyngolaryngeal pain and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: abscess of salivary gland, foaming at mouth, . NEXIUM dosage: unknown. Patient recovered.

Coumadin Side Effects Report #5342438-4
Consumer or non-health professional from UNITED STATES reported COUMADIN problem on May 30, 2007. Female patient, 66 years of age, was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: foaming at mouth, loss of consciousness, . COUMADIN dosage: unknown. During the same period patient was treated with PLAVIX, ASPIRIN, COREG. Patient died on 04/21/2007.

Metoprolol Side Effects Report #5343497-5
METOPROLOL SUCCINATE problem was reported by a Physician from YUGOSLAVIA on May 22, 2007. Female patient, 72 years of age, was diagnosed with dementia alzheimer's type and was treated with METOPROLOL SUCCINATE. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, loss of consciousness, . METOPROLOL SUCCINATE dosage: unknown. During the same period patient was treated with EXELON. Patient recovered.

Metoprolol Side Effects Report #5324823-X
Physician from YUGOSLAVIA reported METOPROLOL SUCCINATE problem on May 08, 2007. Female patient, 73 years of age, was treated with METOPROLOL SUCCINATE. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, loss of consciousness, . METOPROLOL SUCCINATE dosage: unknown. During the same period patient was treated with EXELON. Patient recovered.

Ativan Side Effects Report #5655601-X
ATIVAN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Male patient, 26 years of age, weighting 79.37 lb, was diagnosed with antibiotic prophylaxis and was treated with ATIVAN. After drug was administered, patient experienced the following problems/side effects: chills, foaming at mouth, multi-organ failure, . ATIVAN dosage: unknown. During the same period patient was treated with MORPHINE SULPHATE, BETADINE. Patient died on 02/04/2006.

Betadine Side Effects Report #5655633-1
Consumer or non-health professional from UNITED STATES reported BETADINE SOLUTION problem on Feb 28, 2008. Male patient, 26 years of age, weighting 79.37 lb, was diagnosed with accidental exposure and was treated with BETADINE SOLUTION. After drug was administered, patient experienced the following problems/side effects: chills, foaming at mouth, multi-organ failure, . BETADINE SOLUTION dosage: unknown. During the same period patient was treated with MORPHINE SULPHATE, ATIVAN. Patient died on 02/04/2006.

Actiq Side Effects Report #5677935-5
ACTIQ problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Male patient, 38 years of age, weighting 225.0 lb, was treated with ACTIQ. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, foaming at mouth, hyperhidrosis, narcotic intoxication, nasal mucosal discolouration, oral mucosal discolouration, peripheral coldness, skin discolouration, . ACTIQ dosage: unknown. During the same period patient was treated with PROTONIX, CORTICOSTEROID. Patient died on 02/19/2006.

Omnipaque Side Effects Report #5636027-1
Health Professional from UNITED STATES reported OMNIPAQUE problem on Feb 20, 2008. Female patient was diagnosed with computerised tomogram and was treated with OMNIPAQUE. After drug was administered, patient experienced the following problems/side effects: aphasia, convulsion, foaming at mouth, . OMNIPAQUE dosage: 75 ML ONCE IV. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5602498-X
PAXIL CR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 21, 2008. Female patient, 20 years of age, was diagnosed with depression and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: confusional state, convulsion, foaming at mouth, memory impairment, . PAXIL CR dosage: 50MG TWICE PER DAY. During the same period patient was treated with KEPPRA, XANAX. Patient was hospitalized. Patient recovered.

Strattera Side Effects Report #5533368-3
Physician from UNITED STATES reported STRATTERA problem on Nov 26, 2007. Female patient was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: convulsion, dyspnoea, foaming at mouth, headache, somnolence, . STRATTERA dosage: 25 MG, DAILY (1/D). During the same period patient was treated with PREVACID, RANITIDINE, ATIVAN. Patient recovered.

Optiray Side Effects Report #5570601-6
OPTIRAY problem was reported by a Physician from SPAIN on Dec 10, 2007. Female patient was diagnosed with computerised tomogram thorax and was treated with OPTIRAY. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, convulsion, foaming at mouth, heart rate decreased, . OPTIRAY dosage: 100 ML, SINGLE. Patient died on 12/04/2007.

Forteo Side Effects Report #5577897-5
Consumer or non-health professional from SPAIN reported FORTEO problem on Dec 17, 2007. Female patient, 77 years of age, was diagnosed with osteoporosis, pain, gastric disorder, nervousness, memory impairment and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: amnesia, epilepsy, foaming at mouth, loss of consciousness, . FORTEO dosage: unknown. During the same period patient was treated with ANALGESICS, OMEPRAZOLE, ORFIDAL, CALCIUM, SOMAZINA. Patient was hospitalized. Patient recovered.

Morphine Side Effects Report #5580399-3
MORPHINE SULPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 13, 2007. Male patient, 27 years of age, weighting 380.0 lb, was diagnosed with back pain, headache and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, headache, neck pain, overdose, peripheral coldness, snoring, unresponsive to stimuli, . MORPHINE SULPHATE dosage: unknown. During the same period patient was treated with MORPHINE SULPHATE, MORPHINE SULPHATE, MORPHINE SULPHATE, NORCO, XANAX, KLONOPIN. Patient died on 11/24/2007.

Oxycontin Side Effects Report #5590894-9
Health Professional from UNITED STATES reported OXYCONTIN problem on Aug 14, 2007. Male patient, 19 years of age, weighting 164.9 lb, was diagnosed with alcohol use and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: choking, feeling hot, foaming at mouth, substance abuse, unresponsive to stimuli, . OXYCONTIN dosage: 80 MG, SEE TEXT, INHALATION. During the same period patient was treated with ALCOHOL. Patient died on 09/24/2005.

Lamotrigine Side Effects Report #5511525-X
LAMOTRIGINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 08, 2007. Male patient, 75 years of age, weighting 145.5 lb, was diagnosed with infection, fluid overload, lipids abnormal, chronic obstructive pulmonary disease, heart valve replacement and was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, obstructive airways disorder, tremor, . LAMOTRIGINE dosage: 100MG PER DAY. During the same period patient was treated with CLARITHROMYCIN, ASPIRIN, FUROSEMIDE, SIMVASTATIN, THEOPHYLLINE, BECLAZONE, WARFARIN. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5518823-4
Pharmacist from UNITED KINGDOM reported CLARITHROMYCIN problem on Nov 07, 2007. Male patient, 75 years of age, weighting 145.5 lb, was diagnosed with infection, partial seizures, fluid overload, lipids abnormal, chronic obstructive pulmonary disease, heart valve replacement and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, obstructive airways disorder, tremor, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with LAMOTRIGINE, ACETYLSALICYLIC ACID SRT, FUROSEMIDE, SIMVASTATIN, THEOPHYLLINE, BECLOMETHASONE DIPROPIONATE, WARFARIN, FRUMIL. Patient was hospitalized. Patient recovered.

Magnevist Side Effects Report #5520071-9
MAGNEVIST problem was reported by a Physician from NORWAY on Nov 09, 2007. Male patient, 45 years of age, weighting 209.4 lb, was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: burning sensation, dyspnoea, foaming at mouth, nasal congestion, rash, sneezing, swollen tongue, . MAGNEVIST dosage: 15 ML, 1 DOSE. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5524555-9
Health Professional from UNITED KINGDOM reported CLARITHROMYCIN problem on Nov 07, 2007. Female patient was diagnosed with infection, chronic obstructive pulmonary disease, thrombosis prophylaxis, fluid overload, haemodynamic instability and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, obstructive airways disorder, tremor, . CLARITHROMYCIN dosage: 500 MG, BID. During the same period patient was treated with LAMOTRIGINE, ADRENALINE, DISPERSIBLE ASPIRIN, BECLAZONE, CLEXANE, DOPAMINE, FRUSEMIDE. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5528520-7
CLARITHROMYCIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 06, 2007. Male patient, 75 years of age, was diagnosed with infection and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: convulsion, foaming at mouth, obstructive airways disorder, tremor, . CLARITHROMYCIN dosage: 500MG;TWICE A DAY ORAL. During the same period patient was treated with LAMOTRIGINE, EPINEPHRINE, ASPIRIN, BECLAZONE, ENOXAPARIN, DOPAMINE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5428588-2
Health Professional from UNITED STATES reported OMNISCAN problem on Aug 20, 2007. Male patient, 58 years of age, was diagnosed with abdominal pain, liver function test abnormal and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: communication disorder, dyskinesia, foaming at mouth, gaze palsy, respiratory arrest, . OMNISCAN dosage: 20 ML, SINGLE DOSE, I.V.. Patient died on 08/20/2007.

Morphine Side Effects Report #5436957-X
MORPHINE SULPHATE problem was reported by a Consumer or non-health professional from on Aug 24, 2007. Male patient, 26 years of age, weighting 79.37 lb, was diagnosed with accidental exposure and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: chills, foaming at mouth, multi-organ failure, . MORPHINE SULPHATE dosage: 100 MG, TWICE. During the same period patient was treated with ATIVAN. Patient died on 02/04/2006.

Foradil Side Effects Report #5731535-7
Consumer or non-health professional from UNITED STATES reported FORADIL problem on May 06, 2008. Male patient, 73 years of age, weighting 195.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with FORADIL. After drug was administered, patient experienced the following problems/side effects: brain injury, cardio-respiratory arrest, foaming at mouth, unresponsive to stimuli, . FORADIL dosage: unknown. Patient died on 02/25/2006.

Diazepam Side Effects Report #5744550-4
DIAZEPAM problem was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2008. Male patient, 60 years of age, was diagnosed with cervical spinal stenosis, neck pain, osteochondrosis and was treated with DIAZEPAM. After drug was administered, patient experienced the following problems/side effects: dry mouth, foaming at mouth, gingival pain, gingival pruritus, hernia, jaw disorder, sensory disturbance, . DIAZEPAM dosage: 10 MG; TWICE A DAY; ORAL. During the same period patient was treated with HYDROCODONE, ZETIA, AMBIEN. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5744966-6
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on May 12, 2008. Female patient, weighting 230.0 lb, was diagnosed with fibromyalgia, intervertebral disc protrusion, anxiety and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, disorientation, foaming at mouth, gait disturbance, hyperhidrosis, hypoaesthesia, joint sprain, unresponsive to stimuli, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, CLONAZEPAM, ZANAFLEX, LEXAPRO. Patient recovered.

Fentanyl Side Effects Report #5691264-5
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2008. Female patient, weighting 152.0 lb, was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: arthritis, dysphagia, foaming at mouth, oedema peripheral, pharyngeal oedema, secretion discharge, skin discolouration, throat irritation, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient recovered.

Hydrocodone Side Effects Report #5705168-2
Consumer or non-health professional from UNITED STATES reported HYDROCODONE BITARTRATE problem on Mar 28, 2008. Male patient, 60 years of age, was diagnosed with cervical spinal stenosis, myalgia and was treated with HYDROCODONE BITARTRATE. After drug was administered, patient experienced the following problems/side effects: dry mouth, foaming at mouth, gingival pruritus, hernia, jaw disorder, . HYDROCODONE BITARTRATE dosage: unknown. During the same period patient was treated with VALIUM, TYLENOL W, ZETIA, AMBIEN. Patient was hospitalized. Patient recovered.