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

DYSPNOEA ( 21 FDA reports)
DIZZINESS ( 19 FDA reports)
HEADACHE ( 17 FDA reports)
PAIN ( 16 FDA reports)
ASTHMA ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
FATIGUE ( 12 FDA reports)
STATUS ASTHMATICUS ( 11 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
COUGH ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
VOMITING ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
AGEUSIA ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
FALL ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
ANOSMIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HEREDITARY ANGIOEDEMA ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INJURY ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
INFUSION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
IRITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURNAL FEAR ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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