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Aleve Side Effects Report #5656310-3
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Aug 06, 2007. Male patient, 33 years of age, weighting 200.6 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, hypoaesthesia, pain in extremity, . ALEVE dosage: unknown. During the same period patient was treated with ALLERGY SHOTS. Patient recovered.

Loestrin Side Effects Report #5663154-5
LOESTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, 26 years of age, weighting 130.1 lb, was diagnosed with menstrual cycle management and was treated with LOESTRIN. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, headache, hypoaesthesia facial, muscular weakness, skin discolouration, transient ischaemic attack, vision blurred, . LOESTRIN dosage: unknown. During the same period patient was treated with TOPROL. Patient recovered.

Humira Side Effects Report #5668314-5
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 21, 2008. Male patient, weighting 190.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, oedema peripheral, pain, paraesthesia, . HUMIRA dosage: unknown. Patient recovered.

Ambien Side Effects Report #5616603-2
AMBIEN CR problem was reported by a Health Professional from UNITED STATES on Feb 06, 2008. Female patient, weighting 148.0 lb, was diagnosed with insomnia and was treated with AMBIEN CR. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, muscular weakness, myalgia, . AMBIEN CR dosage: unknown. During the same period patient was treated with AMBIEN CR. Patient recovered.


Vytorin Side Effects Report #5604617-8
Consumer or non-health professional from UNITED STATES reported VYTORIN problem on Jan 24, 2008. Female patient, 49 years of age, weighting 170.0 lb, was diagnosed with blood cholesterol and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, muscular weakness, myalgia, . VYTORIN dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5472746-8
ARIMIDEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2006. Female patient, 48 years of age, was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, . ARIMIDEX dosage: unknown. Patient recovered.

Viagra Side Effects Report #5503236-1
Consumer or non-health professional from UNITED STATES reported VIAGRA problem on Oct 22, 2007. Male patient, weighting 250.0 lb, was diagnosed with erectile dysfunction and was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, hypoaesthesia, hypoaesthesia facial, nerve compression, pain in extremity, sensory loss, . VIAGRA dosage: unknown. During the same period patient was treated with EFFEXOR, LORATADINE, GABAPENTIN, IBUPROFEN, ZOCOR, GLUCOPHAGE, VALSARTAN. Patient recovered.

Aleve Side Effects Report #5752468-6
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 28, 2008. Male patient, 33 years of age, weighting 200.6 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, hypoaesthesia, pain in extremity, . ALEVE dosage: unknown. During the same period patient was treated with ALLERGY SHOTS. Patient recovered.

Omacor Side Effects Report #5372491-3
Consumer or non-health professional from UNITED STATES reported OMACOR problem on May 08, 2007. Male patient, 68 years of age, weighting 182.0 lb, was diagnosed with high density lipoprotein increased and was treated with OMACOR. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, muscle spasms, off label use, pain, treatment noncompliance, . OMACOR dosage: unknown. During the same period patient was treated with DIOVAN, ADVICOR. Patient recovered.


Lipitor Side Effects Report #5316180-X
LIPITOR problem was reported by a Pharmacist from JAPAN on Apr 23, 2007. Female patient, 77 years of age, was diagnosed with hyperlipidaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, pain in extremity, . LIPITOR dosage: DAILY DOSE:10MG. During the same period patient was treated with ANASTROZOLE, AMLODIN, LASIX, ALLELOCK, WARFARIN, FLUTICASONE PROPIONATE, SEREVENT. Patient recovered.

Pravachol Side Effects Report #5629507-6
Consumer or non-health professional from UNITED STATES reported PRAVACHOL problem on Feb 14, 2008. Male patient, 81 years of age, was treated with PRAVACHOL. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, hypoaesthesia, nerve injury, neuropathy peripheral, pain in extremity, peripheral vascular disorder, sleep disorder, tinnitus, . PRAVACHOL dosage: unknown. Patient recovered.

Omniscan Side Effects Report #5588254-X
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on Dec 25, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma, hydrocephalus and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, grip strength decreased, haemodialysis, joint range of motion decreased, musculoskeletal stiffness, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. Patient recovered.

Clonidine Side Effects Report #5545766-2
Physician from IRELAND reported CLONIDINE problem on Nov 27, 2007. Female patient, child 11 years of age, was diagnosed with tourette's disorder and was treated with CLONIDINE. After drug was administered, patient experienced the following problems/side effects: dysarthria, grip strength decreased, heart rate increased, muscular weakness, transient ischaemic attack, . CLONIDINE dosage: unknown. During the same period patient was treated with RISPERIDONE. Patient was hospitalized. Patient recovered.

Amiodarone Side Effects Report #5517837-8
AMIODARONE problem was reported by a Pharmacist from UNITED STATES on Oct 30, 2007. Male patient, 56 years of age, weighting 213.8 lb, was diagnosed with ventricular tachycardia and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: convulsion, grip strength decreased, unresponsive to stimuli, . AMIODARONE dosage: unknown. Patient was hospitalized. Patient recovered.


Fluorouracil Side Effects Report #5483651-5
Consumer or non-health professional from UNITED STATES reported FLUOROURACIL problem on Oct 09, 2007. Female patient, weighting 106.9 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, grip strength decreased, neuropathy, neurotoxicity, . FLUOROURACIL dosage: 2400 MG. During the same period patient was treated with BEVACIZUMAB, LEUCOVORIN CALCIUM, ELOXATIN. Patient recovered.

Celebrex Side Effects Report #5418829-X
CELEBREX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 03, 2006. Female patient, 72 years of age, weighting 125.0 lb, was diagnosed with osteoarthritis and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, grip strength decreased, muscle spasms, oedema peripheral, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Celebrex Side Effects Report #5418829-X
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on Aug 03, 2006. Female patient, 72 years of age, weighting 125.0 lb, was diagnosed with osteoarthritis and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, grip strength decreased, muscle spasms, oedema peripheral, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Risperdal Side Effects Report #5757175-1
RISPERDAL problem was reported by a Physician from IRELAND on May 27, 2008. Female patient, weighting 108.0 lb, was diagnosed with tourette's disorder and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: dysarthria, grip strength decreased, heart rate increased, muscular weakness, sedation, transient ischaemic attack, weight increased, . RISPERDAL dosage: unknown. During the same period patient was treated with CLONIDINE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5769719-4
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Apr 02, 2008. Female patient, weighting 132.1 lb, was diagnosed with rheumatoid arthritis, blood cholesterol increased, gastrooesophageal reflux disease, hypertension, vitamin supplementation and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: gastroenteritis viral, grip strength decreased, joint range of motion decreased, nasal congestion, nasopharyngitis, pain in extremity, rhinorrhoea, . HUMIRA dosage: unknown. During the same period patient was treated with AZATHIOPRINE, FENOFIBRATE, LANSOPRAZOLE, IRBESARTAN, VITAMINS. Patient recovered.


Neostigmine Side Effects Report #5772010-3
NEOSTIGMINE problem was reported by a Pharmacist from UNITED STATES on June 12, 2008. Female patient, 20 years of age, weighting 218.3 lb, was diagnosed with anaesthesia reversal and was treated with NEOSTIGMINE. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, . NEOSTIGMINE dosage: 3 MG ONCE IV. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5780997-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on June 11, 2008. Female patient, weighting 238.2 lb, was diagnosed with rheumatoid arthritis, pain, prophylaxis against gastrointestinal ulcer, vitamin supplementation, muscle spasms and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: grip strength decreased, joint swelling, mobility decreased, musculoskeletal stiffness, oedema peripheral, pain, pain in extremity, . HUMIRA dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, VENLAFAXINE, LANSOPRAZOLE, METHOTREXATE, FOLIC ACID, QUININE, NAPROXEN. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5751703-8
FENTANYL CITRATE problem was reported by a Physician from UNITED STATES on May 12, 2008. Male patient, 74 years of age, was diagnosed with sedation and was treated with FENTANYL CITRATE. After drug was administered, patient experienced the following problems/side effects: dyskinesia, grip strength decreased, hypertension, hypertensive crisis, hypertensive encephalopathy, oxygen saturation decreased, respiratory distress, transient ischaemic attack, . FENTANYL CITRATE dosage: unknown. During the same period patient was treated with BENADRYL, VERSED, CHLORIDE. Patient recovered.

Loestrin Side Effects Report #5751857-3
Consumer or non-health professional from UNITED STATES reported LOESTRIN problem on May 12, 2008. Female patient, 26 years of age, weighting 59.00 lb, was diagnosed with menstrual cycle management and was treated with LOESTRIN. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, grip strength decreased, hypoaesthesia facial, migraine with aura, muscular weakness, oedema peripheral, prothrombin time shortened, skin discolouration, vision blurred, . LOESTRIN dosage: unknown. During the same period patient was treated with TOPROL, COVERA, ALBUTEROL, VERELAN, ACETAMINOPHEN. Patient recovered.

Promethazine Side Effects Report #5361701-4
PROMETHAZINE problem was reported by a Consumer or non-health professional from UNITED STATES on June 15, 2007. Female patient, 42 years of age, weighting 150.0 lb, was diagnosed with procedural nausea and was treated with PROMETHAZINE. After drug was administered, patient experienced the following problems/side effects: discomfort, grip strength decreased, infusion site erythema, infusion site pain, infusion site swelling, vasodilatation, . PROMETHAZINE dosage: 12.5 MG X 1 IVP. Patient recovered.

Fenofibrate Side Effects Report #5364867-5
Health Professional from GERMANY reported FENOFIBRATE problem on June 16, 2007. Male patient, 56 years of age, was diagnosed with hyperlipidaemia and was treated with FENOFIBRATE. After drug was administered, patient experienced the following problems/side effects: dysstasia, grip strength decreased, quadriplegia, . FENOFIBRATE dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE, ALLOPURINOL. Patient recovered.

Omniscan Side Effects Report #5376597-4
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on June 19, 2007. Male patient was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: gait disturbance, grip strength decreased, nephrogenic fibrosing dermopathy, rash, . OMNISCAN dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Seroquel Side Effects Report #5330267-7
Physician from UNITED STATES reported SEROQUEL problem on May 15, 2007. Male patient, 55 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: dysphemia, grip strength decreased, . SEROQUEL dosage: 200 MG TO 300 MG. During the same period patient was treated with LORAZEPAM. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5336849-0
CHANTIX problem was reported by a Health Professional from UNITED STATES on May 24, 2007. Male patient, weighting 154.0 lb, was diagnosed with nicotine dependence and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: gait disturbance, grip strength decreased, pain in extremity, skin exfoliation, . CHANTIX dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5337486-4
Physician from JAPAN reported LIPITOR problem on May 17, 2007. Female patient, 77 years of age, was diagnosed with hyperlipidaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: depression, grip strength decreased, myalgia, pain, pain in extremity, . LIPITOR dosage: DAILY DOSE:10MG. During the same period patient was treated with ANASTROZOLE, AMLODIN, LASIX, ALLELOCK, WARFARIN, FLUTICASONE PROPIONATE, SEREVENT. Patient recovered.

Chantix Side Effects Report #5298294-6
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 05, 2007. Male patient, weighting 220.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: coordination abnormal, grip strength decreased, headache, movement disorder, . CHANTIX dosage: unknown. During the same period patient was treated with OXYCODONE, METHADONE, KLONOPIN, ALBUTEROL, SPIRIVA, ADVAIR DISKUS, TUSSIONEX, TRAZODONE. Patient recovered.

Humira Side Effects Report #5667082-0
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 09, 2008. Female patient, weighting 160.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, grip strength decreased, pain in extremity, procedural complication, . HUMIRA dosage: unknown. Patient recovered.

Amiodarone Side Effects Report #5505069-9
AMIODARONE problem was reported by a Pharmacist from UNITED STATES on Oct 31, 2007. Male patient, 65 years of age, weighting 213.0 lb, was diagnosed with ventricular tachycardia and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: asthenia, convulsion, grip strength decreased, infusion related reaction, lacunar infarction, unresponsive to stimuli, . AMIODARONE dosage: 150MG IV DRIP (DURATION: 2-3 MINUTES OF INFUSION). Patient recovered.

Omniscan Side Effects Report #5401862-1
Consumer or non-health professional from JAPAN reported OMNISCAN problem on July 18, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, gait disturbance, grip strength decreased, haemodialysis, joint range of motion decreased, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. During the same period patient was treated with TAKEPRON OD, MARZULENE, CALCIUM, ISOSORBIDE DINITRATE, ETIZOLAM. Patient recovered.

Exenatide Side Effects Report #5426572-6
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2007. Male patient, 59 years of age, weighting 233.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: amnesia, condition aggravated, grip strength decreased, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with GLUCOPHAGE, CHOLESTYRAMINE, ZETIA, GLIMEPIRIDE, LISINOPRIL. Patient recovered.

Omniscan Side Effects Report #5401862-1
Consumer or non-health professional from JAPAN reported OMNISCAN problem on July 18, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, gait disturbance, grip strength decreased, haemodialysis, joint range of motion decreased, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. During the same period patient was treated with TAKEPRON OD, MARZULENE, CALCIUM, ISOSORBIDE DINITRATE, ETIZOLAM. Patient recovered.

Exenatide Side Effects Report #5426572-6
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2007. Male patient, 59 years of age, weighting 233.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: amnesia, condition aggravated, grip strength decreased, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with GLUCOPHAGE, CHOLESTYRAMINE, ZETIA, GLIMEPIRIDE, LISINOPRIL. Patient recovered.

Seroquel Side Effects Report #5786045-8
Pharmacist from UNITED STATES reported SEROQUEL problem on June 20, 2008. Female patient, weighting 232.0 lb, was diagnosed with bipolar disorder, conduction disorder and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: bradycardia, dizziness, grip strength decreased, hypotension, mental status changes, syncope, . SEROQUEL dosage: 300 MG BEDTIME PO 1 DOSE. During the same period patient was treated with SERTRALINE HYDROCHLORIDE, LITHIUM CARBONATE ER, ARIPIPRAZOLE, OXYBUTYNIN CHLORIDE, DIPHENHYDRAMINE, QUETIAPINE FUMARATE. Patient was hospitalized. Patient recovered.

Levaquin Side Effects Report #5726264-X
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2008. Female patient, 41 years of age, weighting 170.0 lb, was diagnosed with sinusitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, burning sensation, grip strength decreased, joint stiffness, musculoskeletal pain, musculoskeletal stiffness, pain in extremity, . LEVAQUIN dosage: 750MG 1 A DAY PO. Patient recovered.

Lyrica Side Effects Report #5320757-5
Consumer or non-health professional from NETHERLANDS reported LYRICA problem on May 01, 2007. Male patient, weighting 176.4 lb, was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: clumsiness, emotional disorder, grip strength decreased, illusion, sedation, tremor, . LYRICA dosage: unknown. Patient recovered.

Valtrex Side Effects Report #5293538-9
VALTREX problem was reported by a Physician from JAPAN on Apr 10, 2007. Female patient, 66 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: dysarthria, gait disturbance, grip strength decreased, . VALTREX dosage: 500MG TWICE PER DAY. During the same period patient was treated with ALLOPURINOL, ALOSENN, CALTAN, MYSLEE, CALSLOT. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5231457-4
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 15, 2006. Male patient, 59 years of age, weighting 225.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: amnesia, condition aggravated, grip strength decreased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, CHOLESTYRAMINE, ZETIA. Patient recovered.

Velcade Side Effects Report #5261523-9
VELCADE problem was reported by a Physician from JAPAN on Feb 19, 2007. Female patient, 61 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, fall, grip strength decreased, headache, hyperglycaemia, hypotension, iron deficiency anaemia, pyrexia, renal impairment, . VELCADE dosage: 2.10 MG. During the same period patient was treated with DECADRON, BAKTAR, FAMOTIDINE, FERROMIA. Patient recovered.