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Remicade Side Effects Report #5534323-X
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Nov 26, 2007. Male patient was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: sensory loss, . REMICADE dosage: unknown. Patient recovered.

Chantix Side Effects Report #5475101-X
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2007. Female patient, 63 years of age, weighting 164.9 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: sensory loss, stevens-johnson syndrome, . CHANTIX dosage: unknown. During the same period patient was treated with ASCORBIC ACID, CALCIUM. Patient recovered.

Remicade Side Effects Report #5500288-X
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Oct 18, 2007. Male patient was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: sensory loss, . REMICADE dosage: unknown. Patient recovered.

Xenical Side Effects Report #5721768-8
XENICAL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 23, 2008. Male patient, weighting 448.0 lb, was diagnosed with obesity, hypertension, hypothyroidism, epilepsy and was treated with XENICAL. After drug was administered, patient experienced the following problems/side effects: sensory loss, . XENICAL dosage: unknown. During the same period patient was treated with RAMIPRIL, LEVOTHYROXINE, FUROSEMIDE, LAMOTRIGINE, FRISIUM. Patient was hospitalized. Patient recovered.


Cymbalta Side Effects Report #5227542-3
Consumer or non-health professional from UNITED STATES reported CYMBALTA problem on Oct 10, 2006. Male patient, 36 years of age, was diagnosed with back pain and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: sensory loss, . CYMBALTA dosage: 60 MG, ORAL. Patient recovered.

Chantix Side Effects Report #5663251-4
CHANTIX problem was reported by a Health Professional from UNITED KINGDOM on Mar 03, 2008. Male patient, 43 years of age, weighting 211.6 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: paranoia, sensory loss, . CHANTIX dosage: unknown. Patient recovered.

Champix Side Effects Report #5685400-4
Physician from FRANCE reported CHAMPIX problem on Mar 18, 2008. Female patient, 45 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: dissociative identity disorder, sensory loss, . CHAMPIX dosage: unknown. Patient recovered.

Rebif Side Effects Report #5689557-0
REBIF problem was reported by a Health Professional from UNITED STATES on Mar 17, 2008. Male patient, 24 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: optic neuritis, sensory loss, . REBIF dosage: unknown. During the same period patient was treated with ADVAIR, ALBUTEROL INHALER, PLASMA EXCHANGE. Patient was hospitalized. Patient recovered.

Miglitollet Side Effects Report #5584630-X
Physician from JAPAN reported MIGLITOLLET problem on Dec 26, 2007. Female patient, 60 years of age, was diagnosed with diabetes mellitus and was treated with MIGLITOLLET. After drug was administered, patient experienced the following problems/side effects: muscular weakness, sensory loss, . MIGLITOLLET dosage: unknown. During the same period patient was treated with AMARYL. Patient recovered.


Prograf Side Effects Report #5612857-7
PROGRAF problem was reported by a Consumer or non-health professional from COLOMBIA on Jan 21, 2008. Female patient, 34 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: finger deformity, sensory loss, . PROGRAF dosage: unknown. During the same period patient was treated with CELLCEPT, PREDNISOLONE. Patient recovered.

Provigil Side Effects Report #5613674-4
Consumer or non-health professional from UNITED STATES reported PROVIGIL problem on Apr 04, 2006. Female patient was diagnosed with autonomic nervous system imbalance, orthostatic hypotension and was treated with PROVIGIL. After drug was administered, patient experienced the following problems/side effects: hyperthyroidism, sensory loss, stevens-johnson syndrome, . PROVIGIL dosage: unknown. During the same period patient was treated with PROAMATINE, TEGRETOL, IBUPROFEN, RELAFEN, SERZONE, SYNTHROID, TRAZODONE. Patient recovered.

Ultravist Side Effects Report #5534209-0
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Male patient, 67 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: UNIT DOSE: 140 ML. During the same period patient was treated with READI. Patient recovered.

Ultravist Side Effects Report #5535213-9
Health Professional from UNITED STATES reported ULTRAVIST problem on Nov 20, 2007. Female patient, 70 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: UNIT DOSE: 35 ML. Patient recovered.

Ultravist Side Effects Report #5535214-0
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Male patient, 67 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: UNIT DOSE: 140 ML. During the same period patient was treated with READI. Patient recovered.


Ultravist Side Effects Report #5536970-8
Health Professional from UNITED STATES reported ULTRAVIST problem on Nov 20, 2007. Female patient, 70 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: UNIT DOSE: 35 ML. Patient recovered.

Topamax Side Effects Report #5537061-2
TOPAMAX problem was reported by a Physician from GERMANY on Nov 28, 2007. Female patient, weighting 227.1 lb, was diagnosed with epilepsy and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, sensory loss, . TOPAMAX dosage: unknown. Patient recovered.

Ultravist Side Effects Report #5520118-X
Health Professional from UNITED STATES reported ULTRAVIST problem on Nov 09, 2007. Male patient, 67 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: 140 ML,POWER INJECTOR 1.8 ML/SEC. During the same period patient was treated with READI. Patient recovered.

Ultravist Side Effects Report #5521208-8
ULTRAVIST problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 09, 2007. Female patient, 70 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: 35 ML, 1 DOSE. Patient recovered.

Photofrin Side Effects Report #5528524-4
Consumer or non-health professional from CANADA reported PHOTOFRIN problem on Nov 08, 2007. Male patient, 65 years of age, was diagnosed with glioma and was treated with PHOTOFRIN. After drug was administered, patient experienced the following problems/side effects: facial palsy, sensory loss, . PHOTOFRIN dosage: 2MG/KG. During the same period patient was treated with INTRALIPID R. Patient died.


Lyrica Side Effects Report #5531125-5
LYRICA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient, 55 years of age, weighting 119.9 lb, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: gait disturbance, sensory loss, . LYRICA dosage: unknown. During the same period patient was treated with BACLOFEN. Patient recovered.

Rituximab Side Effects Report #5477491-0
Physician from RUSSIAN FEDERATION reported RITUXIMAB problem on Oct 02, 2007. Male patient, weighting 176.4 lb, was diagnosed with b-cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, sensory loss, . RITUXIMAB dosage: 375 MG/M2, UNK. During the same period patient was treated with ENZASTAURIN, GEMCITABINE, OXALIPLATIN. Patient recovered.

Rituximab Side Effects Report #5495389-9
RITUXIMAB problem was reported by a Physician from RUSSIAN FEDERATION on Oct 15, 2007. Male patient, weighting 176.4 lb, was diagnosed with b-cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, sensory loss, . RITUXIMAB dosage: 375 MG/M2, UNK. During the same period patient was treated with ENZASTAURIN, GEMCITABINE, OXALIPLATIN. Patient recovered.

Remicade Side Effects Report #5501501-5
Health Professional from UNITED KINGDOM reported REMICADE problem on Oct 19, 2007. Female patient, 35 years of age, weighting 132.3 lb, was diagnosed with colitis ulcerative, inflammation, arthropathy, pain, arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: paraesthesia, sensory loss, . REMICADE dosage: unknown. During the same period patient was treated with ARCOXIA, FOLIC ACID, METHOTREXATE. Patient recovered.

Topamax Side Effects Report #5446001-6
TOPAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 29, 2007. Female patient, weighting 140.0 lb, was diagnosed with migraine prophylaxis and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: panic attack, sensory loss, . TOPAMAX dosage: unknown. Patient recovered.

Lamivudine Side Effects Report #5456556-3
Consumer or non-health professional from INDIA reported LAMIVUDINE problem on Sept 05, 2007. Male patient, 35 years of age, was diagnosed with hiv infection and was treated with LAMIVUDINE. After drug was administered, patient experienced the following problems/side effects: immune reconstitution syndrome, sensory loss, skin lesion, tuberculoid leprosy, . LAMIVUDINE dosage: unknown. During the same period patient was treated with STAVUDINE, NEVIRAPINE. Patient recovered.

Avastin Side Effects Report #5410237-0
AVASTIN problem was reported by a Health Professional from UNITED KINGDOM on Aug 02, 2007. Female patient, 59 years of age, was diagnosed with retinal neoplasm and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: muscular weakness, sensory loss, . AVASTIN dosage: 2.5 MG, UNK. Patient recovered.

Rebif Side Effects Report #5417956-0
Consumer or non-health professional from UNITED STATES reported REBIF problem on Aug 06, 2007. Female patient, 37 years of age, weighting 150.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Bupivacaine Side Effects Report #5761256-6
BUPIVACAINE problem was reported by a Physician from INDIA on June 04, 2008. Female patient, 38 years of age, was diagnosed with anaesthesia, analgesia and was treated with BUPIVACAINE. After drug was administered, patient experienced the following problems/side effects: peroneal nerve palsy, sensory loss, thermal burn, . BUPIVACAINE dosage: unknown. During the same period patient was treated with PENTAZOCINE LACTATE. Patient recovered.

Ultravist Side Effects Report #5780134-X
Health Professional from UNITED STATES reported ULTRAVIST problem on Nov 20, 2007. Male patient, 67 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: TOTAL DAILY DOSE: 140 ML UNIT DOSE: 150 ML. During the same period patient was treated with READI. Patient recovered.

Ultravist Side Effects Report #5780140-5
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Female patient, 70 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: back pain, sensory loss, . ULTRAVIST dosage: TOTAL DAILY DOSE: 35 ML UNIT DOSE: 150 ML. Patient recovered.

Chantix Side Effects Report #5794083-4
Health Professional from UNITED KINGDOM reported CHANTIX problem on June 16, 2008. Female patient, weighting 154.3 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: cardiovascular disorder, sensory loss, . CHANTIX dosage: unknown. During the same period patient was treated with WARFARIN, ACETAMINOPHEN W, ASPIRIN, ADIZEM, EZETIMIBE. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5754353-2
CHANTIX problem was reported by a Health Professional from UNITED KINGDOM on May 20, 2008. Male patient, 43 years of age, weighting 211.6 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: paranoia, sensory loss, . CHANTIX dosage: unknown. Patient recovered.

Toprol Side Effects Report #5709992-1
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Aug 02, 2007. Male patient, 71 years of age, weighting 229.9 lb, was diagnosed with hypertension and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: pallor, sensory loss, . TOPROL dosage: unknown. During the same period patient was treated with CRESTOR, LISINOPRIL, DIGITEK, METFORMIN, COUMADIN. Patient recovered.

Opana Side Effects Report #5712085-0
OPANA ER problem was reported by a Physician from UNITED STATES on Apr 08, 2008. Male patient was diagnosed with neuropathy peripheral and was treated with OPANA ER. After drug was administered, patient experienced the following problems/side effects: loss of control of legs, sensory loss, . OPANA ER dosage: 10 MG. Patient recovered.

Avonex Side Effects Report #5725791-9
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 17, 2008. Female patient, 60 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: multiple sclerosis relapse, sensory loss, stress, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Lidocaine Side Effects Report #5349846-6
LIDOCAINE problem was reported by a Consumer or non-health professional from on May 31, 2007. Female patient, 49 years of age, was diagnosed with nerve block, sedation and was treated with LIDOCAINE. After drug was administered, patient experienced the following problems/side effects: motor dysfunction, sensory loss, . LIDOCAINE dosage: 400 MG X 1. During the same period patient was treated with MEPIVACAINE, DORMICUM. Patient recovered.

Chantix Side Effects Report #5370310-2
Pharmacist from UNITED STATES reported CHANTIX problem on June 25, 2007. Female patient, 36 years of age, weighting 120.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: disorientation, sensory loss, . CHANTIX dosage: 0.5 MG QD X 3 DAYS THEN BID PO 1 MG BID PO. Patient recovered.

Betaseron Side Effects Report #5340779-8
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on May 18, 2007. Female patient, 41 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: burns third degree, sensory loss, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5290912-1
Health Professional from UNITED STATES reported LIPITOR problem on Mar 28, 2007. Female patient, weighting 162.0 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: neuropathy peripheral, sensory loss, . LIPITOR dosage: unknown. During the same period patient was treated with NORVASC, PREMARIN, VITAMIN CAP, ACETYLSALICYLIC ACID SRT, BENICAR, TOPROL. Patient recovered.

Avastin Side Effects Report #5304513-X
AVASTIN problem was reported by a Health Professional from UNITED KINGDOM on Apr 11, 2007. Female patient, 59 years of age, was diagnosed with retinal neoplasm and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: muscular weakness, sensory loss, . AVASTIN dosage: 2.5 MG, UNK. Patient recovered.

Kivexa Side Effects Report #5670920-9
Health Professional from UNITED KINGDOM reported KIVEXA problem on Mar 13, 2008. Male patient, 29 years of age, was diagnosed with hiv infection and was treated with KIVEXA. After drug was administered, patient experienced the following problems/side effects: blood amylase increased, neuropathy peripheral, sensory loss, . KIVEXA dosage: unknown. During the same period patient was treated with ATAZANAVIR SULPHATE, RITONAVIR, SEPTRIN. Patient recovered.

Prograf Side Effects Report #5671577-3
PROGRAF problem was reported by a Physician from COLOMBIA on Mar 03, 2008. Female patient, 34 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: finger deformity, paraesthesia, sensory loss, . PROGRAF dosage: unknown. During the same period patient was treated with CELLCEPT, PREDNISOLONE, NIFEDIPINE, ASPIRIN, CALCIUM, LYRICA. Patient recovered.

Mirena Side Effects Report #5622698-2
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Feb 08, 2008. Female patient, 24 years of age, was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: loss of consciousness, pulse absent, sensory loss, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5623394-8
BOTOX problem was reported by a Health Professional from UNITED STATES on Feb 05, 2008. Female patient was diagnosed with dystonia, torticollis and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: motor dysfunction, muscular weakness, sensory loss, . BOTOX dosage: unknown. Patient recovered.

Prograf Side Effects Report #5633835-8
Physician from COLOMBIA reported PROGRAF problem on Feb 08, 2008. Female patient, 34 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: finger deformity, paraesthesia, sensory loss, . PROGRAF dosage: unknown. During the same period patient was treated with CELLCEPT, PREDNISOLONE, NIFEDIPINE, ASPIRIN, CALCIUM, LYRICA. Patient recovered.

Tarceva Side Effects Report #5648132-4
TARCEVA problem was reported by a Physician from FRANCE on Feb 15, 2008. Male patient, 44 years of age, was diagnosed with lung adenocarcinoma and was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: paralysis, sensory loss, . TARCEVA dosage: 150 MG, QD, ORAL. During the same period patient was treated with BEVACIZUMAB, GEMCITABINE. Patient recovered.

Lipitor Side Effects Report #5595626-6
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Jan 16, 2008. Male patient, 73 years of age, weighting 165.0 lb, was diagnosed with blood cholesterol abnormal and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: neuropathy peripheral, paraesthesia, sensory loss, . LIPITOR dosage: 10 MG DAILY OPHTHALMIC. Patient recovered.

Humira Side Effects Report #5559521-0
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 05, 2007. Female patient, weighting 132.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: muscular weakness, pain in extremity, sensory loss, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.

Seroquel Side Effects Report #5573479-X
Consumer or non-health professional from UNITED STATES reported SEROQUEL problem on Dec 18, 2007. Male patient, 53 years of age, weighting 201.9 lb, was diagnosed with schizophrenia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: dizziness, loss of consciousness, sensory loss, visual disturbance, . SEROQUEL dosage: 100 MG AM, 300 MG HS.. During the same period patient was treated with LISINOPRIL, ACTOS, METFORMIN. Patient recovered.

Champix Side Effects Report #5514671-X
CHAMPIX problem was reported by a Health Professional from UNITED KINGDOM on Nov 02, 2007. Male patient, 67 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: asthenia, muscular weakness, sensory loss, . CHAMPIX dosage: unknown. During the same period patient was treated with ADALAT, ARTHROTEC, ACETYLSALICYLIC ACID SRT, OLMESARTAN MEDOXOMIL, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5518634-X
Health Professional from DENMARK reported OMNISCAN problem on Oct 29, 2007. Male patient, 58 years of age, weighting 132.3 lb, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: nephrogenic systemic fibrosis, peripheral coldness, sensory loss, . OMNISCAN dosage: unknown. Patient recovered.