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

DRUG INEFFECTIVE ( 18 FDA reports)
DIZZINESS ( 17 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
PAIN ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
FALL ( 8 FDA reports)
FOOD INTERACTION ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
VOMITING ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
TREMOR ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RASH ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COMA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CRYING ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
COW'S MILK INTOLERANCE ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOTOXICOSIS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL CANCER STAGE 0 ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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