Please choose an event type to view the corresponding MedsFacts report:

CONVULSION ( 27 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
TREMOR ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
DEPRESSION ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
RASH ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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