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

INSOMNIA ( 17 FDA reports)
FATIGUE ( 16 FDA reports)
HEADACHE ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
LETHARGY ( 9 FDA reports)
PAIN ( 9 FDA reports)
DRUG DOSE OMISSION ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ACCIDENT ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLISTER ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FALL ( 7 FDA reports)
FOREIGN BODY IN EYE ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
HELMINTHIC INFECTION ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
SCAB ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
IMPULSIVE BEHAVIOUR ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
RHINITIS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SPINAL COLUMN INJURY ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
CHEMICAL BURNS OF EYE ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
EYELID MARGIN CRUSTING ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJURY ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
SCAR ( 4 FDA reports)
SILICOSIS ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
STRESS ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND ( 1 FDA reports)

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