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Duragesic Side Effects Report #5654576-7
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 26, 2008. Female patient, weighting 200.0 lb, was diagnosed with migraine, nausea, pain, gastrooesophageal reflux disease, hypertension, depression and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, hypertension, nephrolithiasis, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, COMPAZINE, FIORICET, PROTONIX, VASOTEC, TENORETIC, CHANTIX, EFFEXOR. Patient recovered.

Duragesic Side Effects Report #5654704-3
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Female patient, weighting 200.0 lb, was diagnosed with migraine, nausea, pain, gastrooesophageal reflux disease, hypertension, depression and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, hypertension, nephrolithiasis, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, COMPAZINE, FIORICET, PROTONIX, VASOTEC, TENORETIC, CHANTIX, EFFEXOR. Patient recovered.

Humira Side Effects Report #5665474-7
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 03, 2007. Female patient, weighting 133.1 lb, was diagnosed with psoriatic arthropathy, thyroid disorder and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . HUMIRA dosage: unknown. During the same period patient was treated with LIOTHYRONINE, METHOTREXATE, FOLIC ACID. Patient recovered.

Humira Side Effects Report #5667638-5
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Female patient, weighting 115.1 lb, was diagnosed with psoriatic arthropathy, psoriasis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . HUMIRA dosage: unknown. Patient recovered.


Duragesic Side Effects Report #5672399-X
Health Professional from UNITED STATES reported DURAGESIC problem on Mar 18, 2008. Female patient, 45 years of age, weighting 180.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, device leakage, skin infection, skin irritation, thermal burn, underdose, withdrawal syndrome, . DURAGESIC dosage: unknown. Patient recovered.

Fentora Side Effects Report #5675987-X
FENTORA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Female patient was diagnosed with pain and was treated with FENTORA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, no therapeutic response, . FENTORA dosage: unknown. During the same period patient was treated with KADIAN. Patient recovered.

Duragesic Side Effects Report #5616423-9
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Jan 29, 2008. Female patient, weighting 187.0 lb, was diagnosed with pain, medical diet, anaemia, restless legs syndrome, blood potassium abnormal and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, diarrhoea, ear pain, muscle spasms, pharyngolaryngeal pain, septic shock, tooth abscess, . DURAGESIC dosage: unknown. During the same period patient was treated with VITAMINS, VITAMIN B, KLONOPIN, POTASSIUM CHLORIDE, LASIX. Patient was hospitalized. Patient recovered.

Vicodin Side Effects Report #5619931-X
VICODIN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 08, 2007. Male patient, weighting 190.2 lb, was diagnosed with breakthrough pain and was treated with VICODIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, stomach discomfort, . VICODIN dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Duragesic Side Effects Report #5636104-5
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 14, 2008. Female patient, weighting 193.0 lb, was diagnosed with pain, thyroid disorder, gastrooesophageal reflux disease, hypersensitivity, depression, blood cholesterol and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, diplopia, dizziness, insomnia, nausea, photopsia, . DURAGESIC dosage: unknown. During the same period patient was treated with SYNTHROID, ATENOLOL, HYDROCHLOROTHIAZIDE, OMEPRAZOLE, ASPIRIN, CLARINEX, FLUOXETINE, ZETIA. Patient recovered.


Tysabri Side Effects Report #5643841-5
TYSABRI problem was reported by a Health Professional from UNITED STATES on Feb 13, 2008. Female patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . TYSABRI dosage: 300 MG, QM, IV. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5585369-7
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Jan 04, 2008. Female patient, weighting 260.0 lb, was diagnosed with intervertebral disc protrusion, mental impairment and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, nausea, pancreatitis, vomiting, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with SEROQUEL. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5591179-7
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Health Professional from UNITED STATES on Jan 03, 2008. Female patient was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, loss of consciousness, pneumonia, pulmonary congestion, pulmonary oedema, respiratory distress, sedation, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PERCOCET. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5594833-6
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Jan 08, 2008. Female patient, weighting 187.0 lb, was diagnosed with pain, medical diet, anaemia, restless legs syndrome, blood potassium abnormal and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, diarrhoea, ear pain, muscle spasms, pharyngolaryngeal pain, septic shock, tooth abscess, . DURAGESIC dosage: unknown. During the same period patient was treated with VITAMINS, VITAMIN B, KLONOPIN, POTASSIUM CHLORIDE, LASIX. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5601274-1
FENTANYL problem was reported by a Health Professional from UNITED STATES on Jan 22, 2008. Female patient, 53 years of age, weighting 327.0 lb, was diagnosed with fibromyalgia, osteonecrosis, pain and was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, inadequate analgesia, . FENTANYL dosage: unknown. Patient recovered.


Dilaudid Side Effects Report #5567314-3
Consumer or non-health professional from UNITED STATES reported DILAUDID problem on Jan 04, 2007. Male patient, weighting 155.1 lb, was diagnosed with pain, gastrooesophageal reflux disease, insomnia and was treated with DILAUDID. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . DILAUDID dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, TERAZOSIN, SIMVASTATIN, QUETIAPINE, ZOLPIDEM TARTRATE. Patient recovered.

Fentanyl Side Effects Report #5567922-X
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 10, 2007. Female patient, weighting 120.0 lb, was diagnosed with trigeminal neuralgia, pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, multiple sclerosis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Duragesic Side Effects Report #5506375-4
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Oct 25, 2007. Female patient, weighting 231.0 lb, was diagnosed with scoliosis, influenza immunisation, depression, blood pressure, anxiety, migraine, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, fatigue, gastrointestinal disorder, glycosylated haemoglobin increased, inflammation, insomnia, menorrhagia, pneumonia, pulmonary oedema, . DURAGESIC dosage: unknown. During the same period patient was treated with FLU SHOT, CYMBALTA, CARDIZEM CD, XANAX, MAXALT, KEPPRA, AXERT, PROTONIX. Patient was hospitalized. Patient recovered.

Wellbutrin Side Effects Report #5507671-7
WELLBUTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient, 64 years of age, was diagnosed with depression, multiple sclerosis, sleep disorder, chronic obstructive pulmonary disease and was treated with WELLBUTRIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, chronic obstructive pulmonary disease, cranial nerve disorder, dyskinesia, dyspnoea, facial pain, neuralgia, pain in jaw, . WELLBUTRIN dosage: unknown. During the same period patient was treated with REBIF, PREDNISONE, FENTANYL, AMBIEN, ADVAIR DISKUS, PROVENTIL, SPIRIVA, RESTORIL. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5530151-X
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Nov 20, 2007. Female patient, weighting 135.0 lb, was diagnosed with osteoarthritis, fibromyalgia and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, constipation, faecaloma, hepatic steatosis, hiatus hernia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, BUMEX. Patient recovered.


Rebif Side Effects Report #5481061-8
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Female patient, 64 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, cranial nerve disorder, dyskinesia, facial pain, obstructive chronic bronchitis with acute exacerbation, pain in jaw, shared psychotic disorder, . REBIF dosage: unknown. During the same period patient was treated with PREDNISONE, WELLBUTRIN, FENTANYL, AMBIEN CR, ADVAIR, PROVENTIL, SPIRIVA, RESTORIL. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5482130-9
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Oct 01, 2007. Male patient was diagnosed with pain, depression, muscle spasms, sleep disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, collapse of lung, convulsion, fall, gallbladder disorder, hypertension, nausea, . DURAGESIC dosage: unknown. During the same period patient was treated with EFFEXOR, BACLOFEN, AMITRIPTYLINE. Patient was hospitalized. Patient recovered.

Lopid Side Effects Report #5483548-0
LOPID problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 10, 2007. Female patient, 38 years of age, weighting 180.0 lb, was diagnosed with blood cholesterol increased and was treated with LOPID. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, condition aggravated, loss of employment, muscle disorder, muscular weakness, myalgia, pain in extremity, . LOPID dosage: 600 MG 2XS DAILY. Patient recovered.

Meperidine Side Effects Report #5484693-6
Physician from UNITED STATES reported MEPERIDINE problem on Sept 27, 2007. Female patient, 44 years of age, was diagnosed with pain, depression and was treated with MEPERIDINE. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, disorientation, illusion, paranoia, platelet count increased, respiratory rate increased, serotonin syndrome, white blood cell count increased, wound infection, . MEPERIDINE dosage: 230 MG TOTAL OVER 8 HOURS, PARENTERAL. During the same period patient was treated with CITALOPRAM HYDROBROMIDE, HYDROMORPHONE, HYDROCODONE BITARTRATE, PROMETHAZINE, GATIFLOXACIN, ZOLPIDEM TARTRATE, LANSOPRAZOLE, ENOXAPARIN. Patient recovered.

Oxycontin Side Effects Report #5487042-2
OXYCONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2007. Male patient was diagnosed with radiculitis brachial, spinal osteoarthritis and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . OXYCONTIN dosage: 80 MG 1 PO Q 8. Patient recovered.

Duragesic Side Effects Report #5487754-0
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Oct 05, 2007. Female patient, weighting 180.0 lb, was diagnosed with rheumatoid arthritis and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, convulsion, diarrhoea, feeling jittery, insomnia, nausea, panic attack, pneumonia viral, pulmonary embolism, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.

Wellbutrin Side Effects Report #5489650-1
WELLBUTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 16, 2007. Female patient, 64 years of age, was diagnosed with depression, multiple sclerosis, sleep disorder, chronic obstructive pulmonary disease and was treated with WELLBUTRIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, chronic obstructive pulmonary disease, cranial nerve disorder, dyskinesia, dyspnoea, psychotic disorder, . WELLBUTRIN dosage: unknown. During the same period patient was treated with REBIF, PREDNISONE, FENTANYL, AMBIEN, ADVAIR DISKUS, PROVENTIL, SPIRIVA, RESTORIL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5493840-1
Physician from UNITED STATES reported REBIF problem on Oct 10, 2007. Female patient, 64 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, chronic obstructive pulmonary disease, cranial nerve disorder, dyskinesia, facial pain, pain in jaw, psychotic disorder, . REBIF dosage: unknown. During the same period patient was treated with PREDNISONE, ADVAIR, PROVENTIL, SPIRIVA, RESTORIL, CARTIA XT, TOPROL, COUMADIN. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5495629-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 15, 2007. Female patient, weighting 165.0 lb, was diagnosed with back pain, sleep disorder, seasonal allergy, sinusitis, arthritis, convulsion and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, convulsion, device leakage, migraine, muscle spasms, neuralgia, palpitations, . DURAGESIC dosage: unknown. During the same period patient was treated with RESTORIL, ALLEGRA D, FLONASE, IBUPROFEN, DILANTIN. Patient recovered.

Requip Side Effects Report #5445384-0
Consumer or non-health professional from UNITED STATES reported REQUIP problem on June 01, 2007. Female patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, therapeutic response decreased, . REQUIP dosage: .5MG AT NIGHT. Patient recovered.

Morphine Side Effects Report #5451565-2
MORPHINE problem was reported by a Consumer or non-health professional from on Sept 06, 2007. Female patient, 45 years of age, was diagnosed with pain, analgesia, musculoskeletal discomfort and was treated with MORPHINE. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, hyperaesthesia, inadequate analgesia, nausea, vomiting, . MORPHINE dosage: unknown. During the same period patient was treated with HYDROMORPHONE, LORAZEPAM, METHADONE, OXYCODONE, GABAPENTIN, FENTANYL TRANSDERMAL SYSTEM. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5463826-1
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Sept 04, 2007. Female patient, 30 years of age, weighting 250.0 lb, was diagnosed with fibromyalgia, pain, systemic lupus erythematosus and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, chills, constipation, dizziness, dysstasia, feeling of body temperature change, hyperhidrosis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Fentanyl Side Effects Report #5472148-4
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient, 69 years of age, weighting 92.00 lb, was diagnosed with abdominal pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, feeling cold, hyperhidrosis, inadequate analgesia, muscle spasms, overdose, tremor, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PLAQUENIL, PREVACID, REGLAN, LIPITOR, ASPIRIN, MIRALAX, KLONOPIN. Patient was hospitalized. Patient recovered.

Gabapentin Side Effects Report #5416473-1
Health Professional from UNITED KINGDOM reported GABAPENTIN problem on Aug 03, 2007. Male patient, 60 years of age, was diagnosed with neuralgia and was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, dysarthria, . GABAPENTIN dosage: unknown. Patient recovered.

Humira Side Effects Report #5764397-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 22, 2008. Female patient was diagnosed with arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, cerebrovascular accident, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5768409-1
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 03, 2008. Male patient, weighting 215.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . HUMIRA dosage: unknown. Patient recovered.

Duragesic Side Effects Report #5793434-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on June 17, 2008. Female patient, weighting 230.0 lb, was diagnosed with pain, chronic obstructive pulmonary disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, chronic obstructive pulmonary disease, kidney infection, lung infection, . DURAGESIC dosage: unknown. During the same period patient was treated with ALBUTEROL, XOPENEX. Patient was hospitalized. Patient recovered.

Avinza Side Effects Report #5750437-3
Consumer or non-health professional from UNITED STATES reported AVINZA problem on Apr 30, 2007. Female patient was diagnosed with pain and was treated with AVINZA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . AVINZA dosage: 30 MG, QD. Patient recovered.

Avinza Side Effects Report #5750458-0
AVINZA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2008. Female patient was diagnosed with pain, muscle spasms, migraine, chronic obstructive pulmonary disease, asthma and was treated with AVINZA. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, dyspnoea, insomnia, palpitations, . AVINZA dosage: 50 MG, EVERY 12 HOURS. During the same period patient was treated with NORCO, ZOLOFT, TOPAMAX, INHALERS. Patient recovered.

Fentanyl Side Effects Report #5711423-2
Physician from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Apr 18, 2008. Female patient, 62 years of age, weighting 135.0 lb, was diagnosed with cancer pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, inadequate analgesia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient recovered.

Oxycontin Side Effects Report #5345555-8
OXYCONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Male patient, weighting 200.0 lb, was diagnosed with accident, tension headache and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, malaise, nervous system disorder, suicide attempt, . OXYCONTIN dosage: 80 MG. QID PO. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5358573-0
Physician from BELGIUM reported DURAGESIC problem on June 06, 2007. Female patient, weighting 99.21 lb, was diagnosed with cancer pain, neoplasm malignant, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, pleurisy, sarcoma, . DURAGESIC dosage: unknown. During the same period patient was treated with CYTOSTATICS. Patient died on 05/20/2007.

Duragesic Side Effects Report #5364972-3
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on June 12, 2007. Female patient, weighting 118.0 lb, was diagnosed with pain, cardiac disorder, nausea, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, gastrooesophageal reflux disease, irritable bowel syndrome, nausea, . DURAGESIC dosage: unknown. During the same period patient was treated with DIGOXIN, PHENERGAN, FIORICET. Patient recovered.

Duragesic Side Effects Report #5321937-5
Pharmacist from AUSTRALIA reported DURAGESIC problem on May 02, 2007. Female patient, weighting 198.4 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . DURAGESIC dosage: unknown. During the same period patient was treated with OXYNORM. Patient recovered.

Cisplatin Side Effects Report #5336852-0
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 24, 2007. Male patient, weighting 179.9 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, mucosal inflammation, nausea, oral pain, stomatitis, vomiting, . CISPLATIN dosage: 200 MG. Patient recovered.

Nexium Side Effects Report #5312055-0
Consumer or non-health professional from UNITED STATES reported NEXIUM problem on Aug 14, 2006. Female patient, 63 years of age, weighting 130.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, . NEXIUM dosage: unknown. During the same period patient was treated with FOSAMAX, ALLEGRA. Patient recovered.

Fentanyl Side Effects Report #5268197-1
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 08, 2007. Male patient, 51 years of age, weighting 225.0 lb, was diagnosed with back injury and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, headache, inadequate analgesia, lethargy, malaise, nausea, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with ENOXAPARIN, WARFARIN, LEVOTHYROXINE. Patient recovered.

Citalopram Side Effects Report #5662373-1
Consumer or non-health professional from UNITED STATES reported CITALOPRAM HYDROBROMIDE problem on Feb 29, 2008. Female patient, 44 years of age, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, breakthrough pain, debridement, depression, serotonin syndrome, surgery, wound infection, . CITALOPRAM HYDROBROMIDE dosage: 40 MG;QD;PO. During the same period patient was treated with PETHIDINE, FENTANYL TRANSDERMAL SYSTEM, HYDROMORPHONE, ACETAMINOPHEN AND HYDROCODONE BITARTRATE, PROMETHAZINE, GATIFLOXACIN, ZOLPIDEM, LANSOPRAZOLE. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5597317-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 11, 2008. Male patient, weighting 265.0 lb, was diagnosed with pain, breakthrough pain, gastrooesophageal reflux disease, multiple allergies, asthma and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: body temperature increased, breakthrough pain, confusional state, intervertebral disc compression, intervertebral disc disorder, mental status changes, withdrawal syndrome, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PERCOCET, PREVACID, ZYRTEC, SINGULAIR, PHENTERMINE. Patient was hospitalized. Patient recovered.

Opana Side Effects Report #5606485-7
Pharmacist from UNITED STATES reported OPANA ER problem on Jan 11, 2008. Male patient, 56 years of age, was diagnosed with pain and was treated with OPANA ER. After drug was administered, patient experienced the following problems/side effects: anorexia, breakthrough pain, convulsion, malaise, muscle disorder, nausea, tinnitus, vomiting, . OPANA ER dosage: 40 MG, 1 TABLET TID. During the same period patient was treated with LIDODERM, OXYCODONE AND ACETAMINOPHEN, ACIPHEX, LUNESTA. Patient recovered.

Duragesic Side Effects Report #5545323-8
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Female patient, weighting 220.0 lb, was diagnosed with back pain, arthralgia, infection, depression, sleep disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: bone pain, breakthrough pain, calcinosis, hypertension, muscle spasms, skin disorder, staphylococcal infection, tooth loss, . DURAGESIC dosage: unknown. During the same period patient was treated with ESTRADIOL, ZOLOFT, FLURAZEPAM. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5560081-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Oct 24, 2007. Female patient, weighting 210.4 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, breakthrough pain, . HUMIRA dosage: unknown. Patient recovered.