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

DRUG INEFFECTIVE ( 17 FDA reports)
NAUSEA ( 13 FDA reports)
HEADACHE ( 11 FDA reports)
VOMITING ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
PAIN ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
STRESS ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RASH ( 5 FDA reports)
TREMOR ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIOPSY LYMPH GLAND ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use