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

NAUSEA ( 29 FDA reports)
DIARRHOEA ( 28 FDA reports)
DIZZINESS ( 24 FDA reports)
DRUG INEFFECTIVE ( 23 FDA reports)
HEADACHE ( 23 FDA reports)
ANXIETY ( 22 FDA reports)
SUICIDAL IDEATION ( 20 FDA reports)
TREMOR ( 19 FDA reports)
SYNCOPE ( 18 FDA reports)
VOMITING ( 18 FDA reports)
FALL ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
INSOMNIA ( 16 FDA reports)
PAIN ( 16 FDA reports)
ABDOMINAL DISCOMFORT ( 15 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
URINARY INCONTINENCE ( 14 FDA reports)
AGGRESSION ( 13 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ASTHENIA ( 11 FDA reports)
DEATH ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
HYPOTENSION ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
POLLAKIURIA ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
DEHYDRATION ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
SUICIDE ATTEMPT ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
CRYING ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MALAISE ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
SCAR ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
ANGER ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
DEPENDENCE ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DEVICE BREAKAGE ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
UNEVALUABLE EVENT ( 6 FDA reports)
UTERINE RUPTURE ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ADHESION ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PARTIAL SEIZURES ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 5 FDA reports)
RASH ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
ILEUS ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MASTITIS ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYCOBACTERIA BLOOD TEST POSITIVE ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
STRESS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD METHAEMOGLOBIN ABSENT ( 3 FDA reports)
BLOOD PRESSURE AMBULATORY DECREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUROFIBROMATOSIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SEROMA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 3 FDA reports)
SURGERY ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COMA ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EHLERS-DANLOS SYNDROME ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MUTISM ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STUPOR ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
CONGENITAL HIP DEFORMITY ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC SYNDROME ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use